The newly added symbols in the 4th edition include symbols for:

 
  • Importer
  • Distributor
  • Model number
  • Country of manufacture
  • Sterilized using vaporized hydrogen peroxide
  • Single sterile barrier system
  • Double sterile barrier system
  • Single sterile barrier system with protective packaging inside
  • Single sterile barrier system with protective packaging outside
  • Contains human blood or plasma derivatives
  • Contains a medicinal substance
  • Contains biological material of animal origin
  • Contains biological material of human origin
  • Contains hazardous substances
  • Contains nano materials
  • Single patient multiple use
  • Patient name
  • Patient identification 
  • Patient information website
  • Health care centre or doctor
  • Date
  • Medical Device
  • Translation
  • Repackaging
  • Unique Device Identifier

These symbols provide a means of conforming to the information to be provided on medical devices in the General Safety and Performance Requirements (GSPRs) of the Medical Device Regulation (MDR 2017/745) and In Vitro Diagnostics Regulation (IVDR 2017/746) and address information required for patient implant cards and unique device identification.

What does this mean to you?

This new edition provides new symbols that will allow you to more easily conform with specific GSPR requirements and will ensure consistency and uniformity across the industry. The ISO organisation does not foresee a transitional period, the standards takes immediate effect.

Should you want to discuss this more in depth with one of our consultants, please do not hesitate to get in touch with us

 

QARAD BV

ISO Certified
ISO 13485 and ISO 27001

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