Imported Medical Device


Technical Requirements
Product technical requirements should be prepared for medical devices to be registered or filed.

Product technical requirements mainly include performance specifications and testing methods of MDs (finished products), where performance specifications refer to functional and safety specifications and other specifications related to quality control.

Guidelines for the compiling of MD product technical requirements


Testing
Registration testing is required for the registration of class II and III medical devices, which should be conducted as per technical requirements of the product by MD testing facilities.

Samples for registration testing should be manufactured in compliance with the requirements of quality management system. Only those that pass registration testing can be proceeded to clinical trials or registration application.

For the filing of class I medical devices, self-test reports can be provided.

Testing ranges of MD testing centers