Document Center List of Standards on Transfusion, Infusion And Injection Equipment Including Blood Packs Syringes, Needles And Catheters, See 11.040.25
ICS Code 11.040.20
Return to ICS Index.Up to Level 2:
The following documents are a part of this series:
ASTM:
- ASTM-51939 - Standard Practice for Blood Irradiation Dosimetry
- ASTM-A908 - Standard Specification for Stainless Steel Needle Tubing
- ASTM-D4774 - Standard Specification for User Applied Drug Labels in Anesthesiology (Withdrawn 2022)
- ASTM-D5090 - Standard Practice for Standardizing Ultrafiltration Permeate Flow Performance Data
- ASTM-D5131 - Standard Guide for Record Keeping for Electrodialysis/Electrodialysis Reversal Systems (Withdrawn 2023)
- ASTM-E1939 - Standard Practice for Blood Irradiation Dosimetry
- ASTM-E2524 - Standard Test Method for Analysis of Hemolytic Properties of Nanoparticles
- ASTM-F1981 - Standard Specification for Suction Catheters for Use in the Respiratory Tract (Withdrawn 2007)
- ASTM-F2077 - Standard Test Methods for Intervertebral Body Fusion Devices
- ASTM-F2079 - Standard Test Method for Measuring Intrinsic Elastic Recoil of Balloon-Expandable Stents
- ASTM-F2081 - Standard Guide for Characterization and Presentation of the Dimensional Attributes of Vascular Stents
- ASTM-F2172 - Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
- ASTM-F2394 - Standard Guide for Measuring Securement of Balloon Expandable Vascular Stent Mounted on Delivery System
- ASTM-F623 - Standard Performance Specification for Foley Catheter
BSI:
- BS-1263-1 - Reusable hypodermic syringes for medical use.
- BS-1619-1 - Specification for Syringes for Use With Insulin of Strengths20, 40 and 80 Units per Mi
- BS-2463 - Specification for transfusion equipment for medical use
- BS-2463-1 - Transfusion equipment for medical use. Specification for collapsible containers for blood and blood components
- BS-2463-2 - Transfusion equipment for medical use. Specification for administration sets
- BS-3263 - Specification for rubber closures for injectable products
- BS-4843 - Specification for sterile intravascular cannula units for single use
- BS-5724-2.16 - Medical electrical equipment. Particular requirements for safety. Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
- BS-7174-5 - Sterile intravascular catheters and ancillary devices for single use. Specification for balloon dilatation catheters
- BS-EN-1283 - Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
- BS-EN-14820 - Single-use containers for human venous blood specimen collection
- BS-EN-1615 - Enteral feeding catheters and enteral giving sets for single use and their connectors. Design and testing
- BS-EN-1616 - Sterile urethral catheters for single use
- BS-EN-1617 - Sterile drainage catheters and accessory devices for single use
- BS-EN-1707 - Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment. Lock fittings
- BS-EN-1733 - Suction Catheters for Use in the Respiratory Tract
- BS-EN-20594-1 - Conical fittings with a 6% (Luer) taper for syringes, needles and certain other medical equipment. General requirements
- BS-EN-28362-1 - Injection containers for injectables and accessories. Injection vials made of glass tubing
- BS-EN-28362-2 - Injection containers for injectables and accessories. Closures for injection vials
- BS-EN-50072 - Medical electrical equipment. Particular requirements for safety. Specification for peritoneal dialysis equipment
- BS-EN-60601-2-16 - Medical electrical equipment
- BS-EN-60601-2-24 - Medical electrical equipment
- BS-EN-60601-2-24-TC - Tracked Changes. Medical electrical equipment
- BS-EN-80369-5 - Small-bore connectors for liquids and gases in healthcare applications
- BS-EN-IEC-60601-2-16 - Medical electrical equipment
- BS-EN-IEC-60601-2-41 - Medical electrical equipment
- BS-EN-IEC-60601-2-41-TC - Tracked Changes. Medical electrical equipment
- BS-EN-ISO-10555-2 - Sterile, single-use intravascular catheters
- BS-EN-ISO-11070 - Sterile single-use intravascular introducers, dilators and guidewires
- BS-EN-ISO-1135-3 - Transfusion equipment for medical use
- BS-EN-ISO-1135-4 - Transfusion equipment for medical use
- BS-EN-ISO-1135-5 - Transfusion equipment for medical use
- BS-EN-ISO-1135-5-TC - Tracked Changes. Transfusion equipment for medical use
- BS-EN-ISO-11608-4 - Needle-based injection systems for medical use. Requirements and test methods
- BS-EN-ISO-13959 - Water for haemodialysis and related therapies
- BS-EN-ISO-15747 - Plastic containers for intravenous injections
- BS-EN-ISO-21649 - Needle-free injection systems for medical use. Requirements and test methods
- BS-EN-ISO-21649-TC - Tracked Changes. Needle-free injection systems for medical use. Requirements and test methods
- BS-EN-ISO-22413 - Transfer sets for pharmaceutical preparations. Requirements and test methods
- BS-EN-ISO-23500 - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
- BS-EN-ISO-23500-1 - Preparation and quality management of fluids for haemodialysis and related therapies
- BS-EN-ISO-23500-2 - Preparation and quality management of fluids for haemodialysis and related therapies
- BS-EN-ISO-23500-3 - Preparation and quality management of fluids for haemodialysis and related therapies
- BS-EN-ISO-23500-5 - Preparation and quality management of fluids for haemodialysis and related therapies
- BS-EN-ISO-26722 - Water treatment equipment for haemodialysis applications and related therapies
- BS-EN-ISO-3826-1 - Plastics collapsible containers for human blood and blood components
- BS-EN-ISO-3826-2 - Plastics collapsible containers for human blood and blood components
- BS-EN-ISO-3826-3 - Plastics collapsible containers for human blood and blood components
- BS-EN-ISO-3826-4 - Plastics collapsible containers for human blood and blood components
- BS-EN-ISO-6009 - Hypodermic needles for single use. Colour coding for identification
- BS-EN-ISO-6710 - Single-use containers for human venous blood specimen collection
- BS-EN-ISO-7886-1 - Sterile hypodermic syringes for single use
- BS-EN-ISO-7886-2 - Sterile hypodermic syringes for single use
- BS-EN-ISO-7886-3 - Sterile hypodermic syringes for single use
- BS-EN-ISO-80369-1-TC - Tracked Changes. Small-bore connectors for liquids and gases in healthcare applications
- BS-EN-ISO-8362-1 - Injection containers and accessories
- BS-EN-ISO-8362-2 - Injection containers and accessories
- BS-EN-ISO-8362-2-TC - Tracked Changes. Injection containers and accessories
- BS-EN-ISO-8362-3 - Injection containers and accessories
- BS-EN-ISO-8362-4 - Injection containers and accessories
- BS-EN-ISO-8362-5 - Injection containers and accessories
- BS-EN-ISO-8362-7 - Injection containers and accessories
- BS-EN-ISO-8536-1 - Infusion equipment for medical use
- BS-EN-ISO-8536-10 - Infusion equipment for medical use
- BS-EN-ISO-8536-10-TC - Tracked Changes. Infusion equipment for medical use
- BS-EN-ISO-8536-11 - Infusion equipment for medical use
- BS-EN-ISO-8536-11-TC - Tracked Changes. Infusion equipment for medical use
- BS-EN-ISO-8536-12 - Infusion equipment for medical use
- BS-EN-ISO-8536-13 - Infusion equipment for medical use
- BS-EN-ISO-8536-14 - Infusion equipment for medical use
- BS-EN-ISO-8536-15 - Infusion equipment for medical use
- BS-EN-ISO-8536-2 - Infusion equipment for medical use
- BS-EN-ISO-8536-2-TC - Tracked Changes. Infusion equipment for medical use
- BS-EN-ISO-8536-3 - Infusion equipment for medical use
- BS-EN-ISO-8536-4 - Infusion equipment for medical use
- BS-EN-ISO-8536-5 - Infusion equipment for medical use
- BS-EN-ISO-8536-8 - Infusion equipment for medical use
- BS-EN-ISO-8536-8-TC - Tracked Changes. Infusion equipment for medical use
- BS-EN-ISO-8536-9 - Infusion equipment for medical use
- BS-EN-ISO-8536-9-TC - Tracked Changes. Infusion equipment for medical use
- BS-EN-ISO-8537-TC - Tracked Changes. Sterile single-use syringes, with or without needle, for insulin
- BS-EN-ISO-8871 - Elastomeric Parts for Aqueous Parenteral Preparations
- BS-EN-ISO-8871-2 - Elastomeric parts for parenterals and for devices for pharmaceutical use
- BS-EN-ISO-8871-3-TC - Elastomeric parts for parenterals and for devices for pharmaceutical use
- BS-EN-ISO-8871-4 - Elastomeric parts for parenterals and for devices for pharmaceutical use
- BS-EN-ISO-8871-5 - Elastomeric parts for parenterals and for devices for pharmaceutical use
- BS-EN-ISO-8871-5-TC - Tracked Changes. Elastomeric parts for parenterals and for devices for pharmaceutical use
- BS-EN-ISO-9187-1 - Injection equipment for medical use
- BS-EN-ISO-9626 - Stainless steel needle tubing for the manufacture of medical devices. Requirements and test methods
- BS-ISO-11040-4 - Prefilled syringes
- BS-ISO-11418-1 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11418-2 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11418-3 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11418-4 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11418-5 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11418-7 - Containers and accessories for pharmaceutical preparations
- BS-ISO-11663 - Quality of dialysis fluid for haemodialysis and related therapies
- BS-ISO-13959 - Water for haemodialysis and related therapies
- BS-ISO-15010 - Disposable hanging devices for transfusion and infusion bottles. Requirements and test methods
- BS-ISO-15375 - Medical infusion bottles. Suspension devices for multiple use. Requirements and test methods
- BS-ISO-22413 - Transfer sets for pharmaceutical preparations. Requirements and test methods
- BS-ISO-23500 - Guidance for the preparation and quality management of fluids for haemodialysis and related therapies
- BS-ISO-26722 - Water treatment equipment for haemodialysis applications and related therapies
- BS-ISO-28620 - Medical devices. Non-electrically driven portable infusion devices
- BS-ISO-28620-TC - Tracked Changes. Medical devices. Non-electrically driven portable infusion devices
- BS-ISO-3826-3 - Plastics Collapsible Containers for Human Blood & Blood Components, Blood Bag Systems
- BS-ISO-6710 - Single-Use Containers for Venous Blood Specimen Collection
- BS-ISO-8536-12 - Infusion equipment for medical use
- BS-ISO-8536-5 - Infusion equipment for medical use. Burette infusion sets for single use, gravity feed
- BS-ISO-8536-6 - Infusion equipment for medical use
- BS-ISO-8536-7 - Infusion equipment for medical use
- PD-CR-13825 - Luer connectors. A report to CEN CHeF from the CEN forum task group 'Luer fittings'
- PD-IEC-62653 - Guideline for safe operation of medical equipment used for haemodialysis treatments
- PD-IEC/PAS-63023 - Medical electrical system. Input interface for haemodialysis equipment for use of external alarming device
- PD-ISO-19727 - Medical devices. Pump tube spallation test. General procedure
- PD-ISO-23128 - Medical devices. Transfusion set and blood bag compatibility test method
IEC:
- IEC-60601-2-16 - Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
- IEC-60601-2-16-RL - Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
- IEC-60601-2-24 - Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers
- IEC-60601-2-40 - Medical electrical equipment - Part 2-40: Particular requirements for the basic safety and essential performance of electromyographs and evoked response equipment
- IEC-60601-2-41 - Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis
- IEC-60601-2-41-AM1 - Amendment 1 - Medical electrical equipment - Part 2-41: Particular requirements for the basic safety and essential performance of surgical luminaires and luminaires for diagnosis
- IEC-62653 - Guideline for safe operation of medical equipment used for haemodialysis treatments
- IEC-62653-RL - Guideline for safe operation of medical equipment used for haemodialysis treatments
- IEC-80369-5 - Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications
- IEC/PAS-63023 - Fibre optic interconnecting devices and passive components - Part 01: Fibre optic connector cleaning methods
ISO:
- ISO-10555-1-1 - - Amendment 1
- ISO-10555-1-2 - Sterile, single-use intravascular catheters - Part 1: General requirementsAmendment 2
- ISO-10555-2 - Sterile, single-use intravascular catheters - Part 2: Angiographic catheters - Corrigendum
- ISO-10555-5-1 - Amendment
- ISO-10985 - Caps made of aluminium-plastics combinations for infusion bottles and injection vials - Requirements and test methods
- ISO-11040-1 - Prefilled syringes - Part 1: Glass cylinders for dental local anaesthetic cartridges
- ISO-11070 - Sterile single-use intravascular introducers, dilators and guidewires
- ISO-1135-1 - Transfusion equipment for medical use -- Part 1: Glass transfusion bottles, closures and caps
- ISO-1135-3 - Transfusion equipment for medical use - Part 3: Blood-taking sets for single use
- ISO-1135-4 - Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed
- ISO-1135-5 - Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus
- ISO-11418-1 - Containers and accessories for pharmaceutical preparations - Part 1: Drop-dispensing glass bottles
- ISO-11418-2 - Containers and accessories for pharmaceutical preparations - Part 2: Screw-neck glass bottles for syrups
- ISO-11418-2-AM1 - - Amendment 1
- ISO-11418-3 - Containers and accessories for pharmaceutical preparations - Part 3: Screw-neck glass bottles (veral) for solid and liquid dosage forms
- ISO-11418-3-AM1 - - Amendment 1
- ISO-11418-5 - Containers and accessories for pharmaceutical preparations - Part 5: Dropper assemblies
- ISO-11418-7 - Containers and accessories for pharmaceutical preparations - Part 7: Screw-neck vials made of glass tubing for liquid dosage forms
- ISO-14972 - Sterile obturators for single use with over-needle peripheral intravascular catheters
- ISO-15010 - Disposable hanging devices for transfusion and infusion bottles -- Requirements and test methods
- ISO-15137 - Self-adhesive hanging devices for infusion bottles and injection vials - Requirements and test methods
- ISO-15375 - Medical infusion bottles - Suspension devices for multiple use - Requirements and test methods
- ISO-15747 - Plastic containers for intravenous injections
- ISO-15759 - Medical infusion equipment - Plastics caps with inserted elastomeric liner for containers manufactured by the blow-fill-seal (BFS) process
- ISO-19727 - Medical devices - Pump tube spallation test - General procedure
- ISO-21649 - Needle-free injection systems for medical use - Requirements and test methods
- ISO-22413 - Transfer sets for pharmaceutical preparations - Requirements and test methods
- ISO-23128 - Medical devices - Transfusion set and blood bag compatibility test method
- ISO-28620 - Medical devices - Non-electrically driven portable infusion devices
- ISO-3826 - Plastics collapsible containers for human blood and blood components
- ISO-3826-1 - Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
- ISO-3826-1-AM1 - - Amendment 1: Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Amendment 1
- ISO-3826-2 - Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets
- ISO-3826-3 - Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
- ISO-3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
- ISO-594-1 - Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment -- Part 1: General requirements
- ISO-594-2 - Conical fittings with 6 % (Luer) taper for syringes, needles and certain other medical equipment -- Part 2: Lock fittings
- ISO-595-1 - Reusable all-glass or metal-and-glass syringes for medical use -- Part 1: Dimensions
- ISO-595-2 - Reusable all-glass or metal-and-glass syringes for medical use -- Part 2: Design, performance requirements and tests
- ISO-6009 - Hypodermic needles for single use - Colour coding for identification
- ISO-6710 - Single-use containers for human venous blood specimen collection
- ISO-7864 - Sterile hypodermic needles for single use - Requirements and test methods
- ISO-7886-1 - Sterile hypodermic syringes for single use - Part 1: Syringes for manual use
- ISO-7886-2 - Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps
- ISO-80369-1 - Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements
- ISO-80369 PACKAGE - ISO 80369 - Liquids and Gases Small Bore Connectors Package
- ISO-8362-1 - Injection containers and accessories - Part 1: Injection vials made of glass tubing
- ISO-8362-1-AM1 - - Amendment 1
- ISO-8362-2 - Injection containers and accessories - Part 2: Closures for injection vials
- ISO-8362-2-AM1 - - Amendment 1: Injection containers and accessories - Part 2: Closures for injection vials - Amendment 1
- ISO-8362-3 - Injection containers and accessories - Part 3: Aluminium caps for injection vials
- ISO-8362-4 - Injection containers and accessories - Part 4: Injection vials made of moulded glass
- ISO-8362-5 - Injection containers and accessories - Part 5: Freeze drying closures for injection vials
- ISO-8362-6 - Injection containers and accessories - Part 6: Caps made of aluminium-plastics combinations for injection vials
- ISO-8362-7 - Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part
- ISO-8536-1 - Infusion equipment for medical use - Part 1: Infusion glass bottles
- ISO-8536-10 - Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment
- ISO-8536-10-RL - Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment (includes Redline Version)
- ISO-8536-11 - Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment
- ISO-8536-1-1 - Amendment 1 Infusion Equipment for Medical Use - Part 1: Infusion Equipment for Medice
- ISO-8536-11-RL - Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment (includes Redline Version)
- ISO-8536-12 - Infusion equipment for medical use - Part 12: Check valves for single use
- ISO-8536-12-AM1 - Infusion equipment for medical use - Part 12: Check valves - Amendment 1
- ISO-8536-13 - Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact
- ISO-8536-14 - Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact
- ISO-8536-15 - Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use
- ISO-8536-15-AM1 - - Amendment 1: Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use - Amendment 1
- ISO-8536-2 - Infusion equipment for medical use - Part 2: Closures for infusion bottles
- ISO-8536-3 - Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles
- ISO-8536-3-AM1 - - Amendment 1: Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles - Amendment 1
- ISO-8536-4 - Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed
- ISO-8536-4-AM1 - - Amendment 1
- ISO-8536-5 - Infusion equipment for medical use - Part 5: Burette infusion sets for single use, gravity feed
- ISO-8536-6 - Infusion equipment for medical use - Part 6: Freeze drying closures for infusion bottles
- ISO-8536-7 - Infusion equipment for medical use - Part 7: Caps made of aluminium-plastics combinations for infusion bottles
- ISO-8536-8 - Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus
- ISO-8536-8-RL - Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus (includes Redline Version)
- ISO-8536-9 - Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment
- ISO-8536-9-RL - Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (includes Redline Version)
- ISO-8537-1 - AMENDMENT 1
- ISO-8871 - Elastomeric Parts for Aqueous Parenteral Preparations
- ISO-8871-1 - Elastomeric parts for parenterals and for devices for pharmaceutical use -- Part 1: Extractables in aqueous autoclavates
- ISO-8871-2 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization
- ISO-8871-2-AM1 - Elastomeric parts for parenterals and for devices for pharmaceutical use -- Part 2: Identification and characterization - Amendment 1
- ISO-8871-3 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count
- ISO-8871-3-AM1 - - Amendment 1
- ISO-8871-4 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods
- ISO-8871-5 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
- ISO-8872 - Aluminium caps and aluminium/plastic caps for infusion bottles and injection vials - General requirements and test methods
- ISO-9187-1 - Injection equipment for medical use - Part 1: Ampoules for injectables
- ISO-9187-2 - Injection equipment for medical use - Part 2: One-point-cut (OPC) ampoules
- ISO-9626 - Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods
- ISO-9626-1 - Amendment 1
- ISO-9997 - Dentistry - Cartridge syringes
Other SDOs:
- AAMI/IEC-60601-2-16 - Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of hemodialysis, hemodiafiltration and hemofiltration equipment
- AAMI/IEC-60601-2-16-RL - Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of hemodialysis, hemodiafiltration and hemofiltration equipment - Redline Edition
- AAMI/ISO-80369-1 - Small bore connectors for liquids and gases in healthcare applications - Part 1: General requirements.
- DIN-EN-14820 - Single-Use Containers for Human Venous Blood Specimen Collection
- DIN-EN-1733 - Suction catheters for use in the respiratory tract; German version EN 1733:2002
- DIN-EN-ISO-1135-4 - Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed
- DIN-EN-ISO-15747 - Plastic containers for intravenous injections (ISO 15747:2010)
- DIN-EN-ISO-21649 - Needle-Free Injectors for Medical Use - Requirements & Test Methods
- DIN-EN-ISO-3826-1 - Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
- DIN-EN-ISO-8536-10 - Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment
- DIN-EN-ISO-8536-11 - Part 11: Infusion Filters for Use With Pressure Infusion Equipment, Infusion Equipment
- DIN-EN-ISO-8536-4 - Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2010 + Amd 1:2013)
- DIN-EN-ISO-8536-8 - Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus
- DIN-EN-ISO-8536-9 - Part 9: Fluid Lines for Use With Pressure Infusion Equipment, Infusion Equipment for M
- DIN-EN-ISO-8871-4 - Part 4: Biological Requirements and Test Methods, Elastomeric Parts for Parenterals and F
- DIN-ISO-15137 - Self-Adhesive Hanging Devices for Infusion Bottles & Injection Vials - Requirements &
- DIN-ISO-15375 - Medical infusion bottles - Suspension devices for multiple use - Requirements and test methods
- DIN-ISO-15759 - Medical Infusion Equipment - Plastics Caps With Inserted Elastomeric Liner for Contain
- DIN-ISO-8362-7 - Part 7: Injection Caps Made of ALUMINIUM-Plastics Combinations Without Overlapping Pla
- DIN-ISO-8536-5 - Part 5: Burette Infusion Sets for Single Use, Gravity Feed, Infusion Equipment for Me
- EN-14820 - Single-Use Containers for Human Venous Blood, Specimen Collection
- EN-50072 - Section 2.29 Specification for Peritoneal Dialysis Equipment, Part 2: Particular Requi
- EN-60601-2-16 - Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
- EN-60601-2-24 - Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers
- EN-60601-2-41 - Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis
- EN-80369-5 - Small-bore connectors for liquids and gases in healthcare applications - Part 5: Connectors for limb cuff inflation applications
- EN-IEC-60601-2-16 - Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:2018)
- EN-ISO-1135-3 - Transfusion equipment for medical use - Part 3: Blood-taking sets for single use
- EN-ISO-1135-4 - Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed
- EN-ISO-1135-5 - Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus
- EN-ISO-11608-4 - Pen-Injectors for Medical Use, Requirements & Test Methods for Electronic & Electromec
- EN-ISO-15747 - Plastic containers for intravenous injections
- EN-ISO-21649 - Needle-Free Injectors for Medical Use - Requirements & Test Methods
- EN-ISO-3826-1 - Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
- EN-ISO-3826-2 - Plastics Collapsible Containers for Human Blood & Blood Components, Graphical Symbols
- EN-ISO-3826-3 - Plastics Collapsible Containers for Human Blood & Blood Components, Blood Bag Systems
- EN-ISO-3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
- EN-ISO-6710 - Single-use containers for human venous blood specimen collection
- EN-ISO-80369-1 - Small bore connectors for liquids and gases in healthcare applications - Part 1: General requirements
- EN-ISO-8362-1 - Part 1: Injection Vials Made of Glass Tubing, Injection Containers & Accessories
- EN-ISO-8362-2 - Injection containers and accessories - Part 2: Closures for injection vials
- EN-ISO-8362-4 - Injection containers and accessories - Part 4: Injection vials made of moulded glass
- EN-ISO-8362-5 - Injection containers and accessories - Part 5: Freeze drying closures for injection vials
- EN-ISO-8362-6 - Injection containers and accessories - Part 6: Caps made of aluminium-plastics combinations for injection vials
- EN-ISO-8362-7 - Part 7: Injection Caps Made of ALUMINIUM-Plastics Combinations Without Overlapping Pla
- EN-ISO-8536-1 - Infusion equipment for medical use - Part 1: Infusion glass bottles
- EN-ISO-8536-10 - Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment
- EN-ISO-8536-11 - Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment
- EN-ISO-8536-13 - Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact
- EN-ISO-8536-2 - Part 2: Closures for Infusion Bottles, Infusion Equipment for Medical Use
- EN-ISO-8536-3 - Part 3: Aluminium Caps for Infusion Bottles, Infusion Equipment for Medical Use
- EN-ISO-8536-4 - Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2010)
- EN-ISO-8536-5 - Infusion equipment for medical use - Part 5: Burette infusion sets for single use, gravity feed (ISO 8536-5:2004)
- EN-ISO-8536-8 - Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus
- EN-ISO-8536-9 - Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment
- EN-ISO-8871-2 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - Amendment 1
- EN-ISO-8871-4 - Part 4: Biological Requirements & Test Methods, Elastomeric Parts for Parenterals & F
- EN-ISO-8871-5 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing
- EN-ISO-9187-1 - Part 1: Ampoules for Injectables, Injection Equipment for Medical Use
- JIS-T-3211 - Sterile infusion administration set
- JIS-T-3211-10 - Sterile infusion administration set -- Part 10: Sterile accessories for fluid lines for single use
- JIS-T-3211-11 - Sterile infusion administration set -- Part 11: Sterile infusion filters for single use
- JIS-T-3211-12 - Sterile infusion administration set -- Part 12: Sterile check valves for single use
- JIS-T-3211-4 - Sterile infusion administration set -- Part 4: Sterile infusion sets for single use, gravity feed
- JIS-T-3211-5 - Sterile infusion administration set -- Part 5: Sterile burette infusion sets for single use
- JIS-T-3211-8 - Sterile infusion administration set -- Part 8: Sterile infusion sets for single use with pressure infusion apparatus
- JIS-T-3211-9 - Sterile infusion administration set -- Part 9: Sterile fluid lines for single use
- JIS-T-3212 - Sterile blood transfusion set
- JIS-T-3212-4 - Sterile blood transfusion set -- Part 4: Sterile transfusion sets for single use, gravity feed
- JIS-T-3212-5 - Sterile blood transfusion set -- Part 5: Sterile transfusion sets for single use with pressure infusion apparatus
- JIS-T-3217 - Plastic collapsible containers for human blood and blood components
- JIS-T-3219 - Sterile infusion filter
- JIS-T-3220 - Sterile blood collection needles
- JIS-T-3224 - Sterile syringe filter
- JIS-T-3225 - Sterile transfusion filter
- JIS-T-3226-1 - Needle-based injection systems for medical use -- Part 1: Needle-based injection systems -- Requirements and test methods
- JIS-T-3233 - Evacuated single-use containers for venous blood specimen collection
- JIS-T-3242 - The guide wire for non-vascular use
- SIS-EN-60601-2-41 - Medical electrical equipment - Part 2-41: Particular requirements for basic safety and essential performance of surgical luminaires and luminaires for diagnosis - Swedish standard, English language edition
- SS-EN-12439 - Sterile rectal catheters for single use
- SS-EN-1283 - Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
- SS-EN-13867 - Concentrates for haemodialysis and related therapies
- SS-EN-13868 - Catheters - Test methods for kinking of single lumen catheters and medical tubing
- SS-EN-14820 - Single-use containers for human venous blood specimen collection
- SS-EN-1615 - Enteral feeding catheters and enteral giving sets for single use and their connectors - Design and testing
- SS-EN-1616 - Sterile urethal catheters for single use
- SS-EN-1616-AM1 - Sterile urethral catheters for single use
- SS-EN-1617 - Sterile drainage catheters and accessory devices for single use
- SS-EN-1618 - Catheters other than intravascular catheters - Test methods for common properties
- SS-EN-1707 - Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Lock fittings
- SS-EN-20594-1 - Conical fittings with a 6 % (Luer) taper for syringes, needles and certain other medical equipment - Part 1: General requierments (ISO 594-1:1986)
- SS-EN-28362-1 - Injection containers and accessories - Part 1: Injection vials made of glass tubing (ISO 8362-1:2003)
- SS-EN-28362-2 - Injection containers for injectables an accessories - Part 2: Closures for injection vials (ISO 8362-2:1988)
- SS-EN-28362-3 - Injection containers for injectables and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:1989)
- SS-EN-28362-4 - Injection containers for injectables and accessories - Part 4: Injection vials made of moulded glass (ISO 8362-4:1989)
- SS-EN-28872 - Aluminium caps for transfusion, infusion and injection bottles - General requirements and test methods (ISO 8872:1988)
- SS-EN-60601-2-16 - Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
- SS-EN-60601-2-24 - Medical electrical equipment - Part 2-24: Particular requirements for the basic safety and essential performance of infusion pumps and controllers
- SS-EN-62353 - Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
- SS-EN-62366-1 - Medical devices - Part 1: Application of usability engineering to medical devices
- SS-EN-ISO-10555-1 - Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements (ISO 10555-1:2013, Corrected version 2013-07-01)
- SS-EN-ISO-10555-1-AM1 - Intravascular catheters - Sterile and single-use catheters - Part 1: General requirements - Amendment 1 (ISO 10555-1:2013/Amd 1:2017)
- SS-EN-ISO-10555-2 - Sterile, single-use intravascular catheters - Part 2: Angiographic catheters (ISO 10555-2:1996)
- SS-EN-ISO-10555-3 - Intravascular catheters - Sterile and single-use catheters - Part 3: Central venous catheters (ISO 10555-3:2013)
- SS-EN-ISO-10555-4 - Intravascular catheters - Sterile and single-use catheters - Part 4: Balloon dilatation catheters (ISO 10555-4:2013)
- SS-EN-ISO-10555-5 - Intravascular catheters - Sterile and single-use catheters - Part 5: Over-needle peripheral catheters (ISO 10555-5:2013)
- SS-EN-ISO-11070 - Sterile single-use intravascular introducers, dilators and guidewires (ISO 11070:2014)
- SS-EN-ISO-11070-AM1 - Sterile single-use intravascular introducers, dilators and guidewires - Amendment 1 (ISO 11070:2014/Amd 1:2018)
- SS-EN-ISO-1135-3 - Transfusion equipment for medical use - Part 3: Blood-taking sets for single use (ISO 1135-3:2016)
- SS-EN-ISO-1135-4 - Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015)
- SS-EN-ISO-1135-5 - Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015)
- SS-EN-ISO-11608-1 - Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems (ISO 11608-1:2022)
- SS-EN-ISO-11608-2 - Needle-based injection systems for medical use - Requirements and test methods - Part 2: Double-ended pen needles (ISO 11608-2:2022)
- SS-EN-ISO-11608-3 - Needle-based injection systems for medical use - Requirements and test methods - Part 3: Containers and integrated fluid paths (ISO 11608-3:2022)
- SS-EN-ISO-11608-5 - Needle-based injection systems for medical use - Requirements and test methods - Part 5: Automated functions (ISO 11608-5:2022)
- SS-EN-ISO-13958 - Concentrates for haemodialysis and related therapies (ISO 13958:2014)
- SS-EN-ISO-15747 - Plastic containers for intravenous injections (ISO 15747:2018)
- SS-EN-ISO-21649 - Needle-free injectors for medical use - Requirements and test methods (ISO 21649:2006)
- SS-EN-ISO-22413 - Transfer sets for pharmaceutical preparations - Requirements and test methods (ISO 22413:2021)
- SS-EN-ISO-23500-4 - Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)
- SS-EN-ISO-3826-1 - Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
- SS-EN-ISO-3826-1-AM1 - Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Amendment 1 (ISO 3826-1:2019/Amd1:2023)
- SS-EN-ISO-3826-2 - Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets (ISO 3826-2:2008)
- SS-EN-ISO-3826-3 - Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)
- SS-EN-ISO-3826-4 - Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)
- SS-EN-ISO-595-2 - Reusable all-glass or metal-and-glass syringes for medical use - Part 2: Design, performance requirements and tests (ISO 595-2:1987)
- SS-EN-ISO-6009 - Hypodermic needles for single use - Colour coding for identification (ISO 6009:2016)
- SS-EN-ISO-6710 - Single-use containers for human venous blood specimen collection (ISO 6710:2017)
- SS-EN-ISO-7864 - Sterile hypodermic needles for single use - Requirements and test methods (ISO 7864:2016)
- SS-EN-ISO-7885 - Dentistry - Sterile injection needles for single use (ISO 7885:2010)
- SS-EN-ISO-7886-1 - Sterile hypodermic syringes for single use - Part 1: Syringes for manual use (ISO 7886-1:2016)
- SS-EN-ISO-7886-2 - Sterile hypodermic syringes for single use - Part 2: Syringes for use with power-driven syringe pumps (ISO 7886-2:2020)
- SS-EN-ISO-7886-3 - Sterile hypodermic syringes for single use - Part 3: Auto-disabled syringes for fixed-dose immunization (ISO 7886-3:2020)
- SS-EN-ISO-7886-4 - Sterile hypodermic syringes for single use - Part 4: Syringes with re-use prevention feature (ISO 7886-4:2018)
- SS-EN-ISO-80369-1 - Small-bore connectors for liquids and gases in healthcare applications - Part 1: General requirements (ISO 80369-1:2018)
- SS-EN-ISO-8362-1 - Injection containers and accessories - Part 1: Injection vials made of glass tubing (ISO 8362-1:2018)
- SS-EN-ISO-8362-2 - Injection containers and accessories - Part 2: Closures for injection vials (ISO 8362-2:2015)
- SS-EN-ISO-8362-2-AM1 - Injection containers and accessories - Part 2: Closures for injection vials - Amendment 1 (ISO 8362-2:2015/Amd 1:2022)
- SS-EN-ISO-8362-3 - Injection containers and accessories - Part 3: Aluminium caps for injection vials (ISO 8362-3:2001)
- SS-EN-ISO-8362-4 - Injection containers and accessories - Part 4: Injection vials made of moulded glass (ISO 8362-4:2011)
- SS-EN-ISO-8362-5 - Injection containers and accessories - Part 5: Freeze drying closures for injection vials (ISO 8362-5:2016)
- SS-EN-ISO-8362-6 - Injection containers and accessories - Part 6: Caps made of aluminium-plastics combinations for injection vials (ISO 8362-6:2010)
- SS-EN-ISO-8362-7 - Injection containers and accessories - Part 7: Injection caps made of aluminium-plastics combinations without overlapping plastics part (ISO 8362-7:2006)
- SS-EN-ISO-8536-1 - Infusion equipment for medical use - Part 1: Infusion glass bottles (ISO 8536-1:2011)
- SS-EN-ISO-8536-10 - Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment (ISO 8536-10:2015)
- SS-EN-ISO-8536-11 - Infusion equipment for medical use - Part 11: Infusion filters for single use with pressure infusion equipment (ISO 8536-11:2015)
- SS-EN-ISO-8536-13 - Infusion equipment for medical use - Part 13: Graduated flow regulators for single use with fluid contact (ISO 8536-13:2016)
- SS-EN-ISO-8536-14 - Infusion equipment for medical use - Part 14: Clamps and flow regulators for transfusion and infusion equipment without fluid contact (ISO 8536-14:2016)
- SS-EN-ISO-8536-15 - Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use (ISO 8536-15:2022)
- SS-EN-ISO-8536-15-AM1 - Infusion equipment for medical use - Part 15: Light-protective infusion sets for single use - Amendment 1 (ISO 8536-15:2022/Amd 1:2023)
- SS-EN-ISO-8536-2 - Infusion equipment for medical use - Part 2: Closures for infusion bottles (ISO 8536-2:2010)
- SS-EN-ISO-8536-3 - Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles (ISO 8536-3:2009)
- SS-EN-ISO-8536-3-AM1 - Infusion equipment for medical use - Part 3: Aluminium caps for infusion bottles - Amendment 1 (ISO 8536-3:2009/Amd 1:2022)
- SS-EN-ISO-8536-4 - Infusion equipment for medical use - Part 4: Infusion sets for single use, gravity feed (ISO 8536-4:2019)
- SS-EN-ISO-8536-5 - Infusion equipment for medical use - Part 5: Burette infusion sets for single use, gravity feed (ISO 8536-5:2004)
- SS-EN-ISO-8536-8 - Infusion equipment for medical use - Part 8: Infusion sets for single use with pressure infusion apparatus (ISO 8536-8:2015)
- SS-EN-ISO-8536-9 - Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment (ISO 8536-9:2015)
- SS-EN-ISO-8537 - Sterile single-use syringes, with or without needle, for insulin (ISO 8537:2016)
- SS-EN-ISO-8537-AM1 - Sterile single-use syringes, with or without needle, for insulin (ISO 8537:1991/Amd 1:2000)
- SS-EN-ISO-8637 - Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)
- SS-EN-ISO-8637-2 - Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
- SS-EN-ISO-8638 - Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
- SS-EN-ISO-8871 - Elastomeric parts for aqueous parenteral preparations (ISO 8871:1990+Amd 1:1999)
- SS-EN-ISO-8871-2 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization (ISO 8871-2:2020)
- SS-EN-ISO-8871-2-AM1 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 2: Identification and characterization - Amendment 1 (ISO 8871-2:2003/Amd 1:2005)
- SS-EN-ISO-8871-3 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count (ISO 8871-3:2003)
- SS-EN-ISO-8871-3-AM1 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 3: Determination of released-particle count - Amendment 1 (ISO 8871-3:2003/Amd 1:2018)
- SS-EN-ISO-8871-4 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 4: Biological requirements and test methods (ISO 8871-4:2006)
- SS-EN-ISO-8871-5 - Elastomeric parts for parenterals and for devices for pharmaceutical use - Part 5: Functional requirements and testing (ISO 8871-5:2016)
- SS-EN-ISO-8872 - Aluminium caps and aluminium/plastic caps for infusion bottles and injection vials - General requirements and test methods (ISO 8872:2022)
- SS-EN-ISO-9187-1 - Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2010)
- SS-EN-ISO-9187-2 - Injection equipment for medical use - Part 2: One-point-cut (OPC) ampoules (ISO 9187-2:2010)
- SS-EN-ISO-9626 - Stainless steel needle tubing for the manufacture of medical devices - Requirements and test methods (ISO 9626:2016)
- UNE-EN-ISO-1135-4 - Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed
- UNE-EN-ISO-1135-5 - Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus