SS-EN-1041 Information supplied by the manufacturer of medical devices

SS-EN-1041 - 2008/A1 EDITION - SUPERSEDED
Show Complete Document History

Document Center Inc. is an authorized dealer of SIS standards.
The following bibliographic material is provided to assist you with your purchasing decision:


Standarden anger krav på information som ska lämnas av tillverkare av medicintekniska produkter, så som bruksanvisning, märkning och identifiering av produkten. Den är tillämplig på produkter som regleras i EU- direktiven för medicintekniska produkter och aktiva medicintekniska produkter för implantation. Standarden förtydligar de mest väsentliga krav som anges i direktiven och ger dig vägledning om hur dessa kan uppfyllas. This standard specifies requirements for information to be supplied by a manufacturer for medical devices regulated by Council Directive 90/385/EEC relating to active implantable medical devices and Council Directive 93/42/EEC concerning medical devices. It does not specify the language to be used for such information, nor does it specify the means by which the information is to be supplied. It is also intended to complement the specific requirements of the cited EU Directives on medical devices by providing guidance on means by which certain requirements can be met. If a manufacturer follows these means, they will provide a presumption of conformity with the relevant Essential Requirements regarding information to be supplied. This standard does not cover requirements for provision of information for in vitro diagnostic medical devices, which are covered by other labelling standards (see Bibliography). NOTE When national transpositions of the Directives specify the means by which information shall be supplied, this standard does not provide derogation from these requirements for that country.

To find similar documents by classification:

01.110 (Technical product documentation Including rules for preparation of user guides, manuals, product specifications, etc.)

11.040.01 (Medical equipment in general)

11.120.01 (Pharmaceutics in general)


Active implantable medical devices. Medical devices

This document comes with our free Notification Service, good for the life of the document.

This document is available in either Paper or PDF format.

 

Customers who bought this document also bought:

ASTM-D4169
Standard Practice for Performance Testing of Shipping Containers and Systems

ASTM-F1980
Standard Guide for Accelerated Aging of Sterile Barrier Systems and Medical Devices

ASTM-F88
Standard Test Method for Seal Strength of Flexible Barrier Materials




Designation Name

SS-EN 1041:2008

Revision Level

2008/A1 EDITION

Status

Superseded

Publication Date

Sept. 30, 2013

International Equivalent

EN 1041:2008(IDT)