Commission Addresses Non-EU/EEA Authorities To Set Record Straight On New EU Regs
Commission Addresses Non-EU/EEA Authorities To Set Record Straight On New EU Regs
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Hoping to head off possible rejection of IVDs and medical devices by other countries for items receiving CE marks under the European Union’s Directives for medical devices, the European Commission has issued a fact sheet for third-countries that explains the issue.
Author: Amanda Maxwell
Publisher: Medtech
- Description
In an effort to educate worldwide medtech authorities about EU procedures relating to products that were certified under its Directives and Regulations, the European Commission has issued a new factsheet outlining key details on these points. The bottom line: some devices with Directives certification may be sold on the market until May of 2024, and made available until May of 2025. Find out more about how the European Commission is attempting to educate third-countries on devices and IVDs that have been CE marked under Directives from the EU in this informative Medtech Insight article.
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