Taiwan FDA registration c64c46158178864db5b0f7fc4fd19f7b
GEZEN Cervical Cage
TW: 際仁頸椎融合裝置
Taiwan·Risk Class 2·MD·BIOLIFE MEDICAL DEVICE INC.·Registered Jul 19, 2016 – Jul 19, 2026ExpiredRegistration details
- Analysis ID
- c64c46158178864db5b0f7fc4fd19f7b
- License Form
- Ministry of Health Medical Device Manufacturing No. 005384
Company information
- Manufacturer
- BIOLIFE MEDICAL DEVICE INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- BIOLIFE MEDICAL DEVICE INC.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3080 Interbody fusion device
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Jul 19, 2016
- Expiry Date
- Jul 19, 2026
About this record
Access comprehensive regulatory information for GEZEN Cervical Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c64c46158178864db5b0f7fc4fd19f7b and manufactured by BIOLIFE MEDICAL DEVICE INC.. The authorized representative in Taiwan is BIOLIFE MEDICAL DEVICE INC..
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