CDFA Released Technical Guidelines for The Registration of Animal-Derived Medical DevicesJanuary 24, 2018
Key Aspects to Expedite Your Medical Device’s Approval with CFDAJanuary 26, 2018
China Med Device publishes weekly CFDA updates covering medical device regulation, guideline, standard, recall, adverse event alert, recall, registration approval.
Below are the CFDA updates from January 14 to January 20, 2018
- On January 16, 2018, the CFDA issued an adverse event alert on disposable delivery kit.
- On January 18th, 2018, the CFDA issued an adverse event alert on powdered medical groves.
- On Jan 19, the CFDA granted an approval for epidermal growth factor receptor (EGFR) mutation test kit.
- From Jan 14th to Jan 20th, CFDA issued recall alerts on 22 medical devices including Acetabular System by Smith & Nephew, Soft Contact Lens by Johnson & Johnson, etc.