Taiwan FDA registration 4f6fca5f453c8ad4275f51d16050a3a4
GEZEN Lumbar Cage
TW: 際仁腰椎融合裝置
Taiwan·Risk Class 2·MD·BIOLIFE MEDICAL DEVICE INC.·Registered Aug 24, 2016 – Aug 24, 2026ActiveRegistration details
- Analysis ID
- 4f6fca5f453c8ad4275f51d16050a3a4
- License Form
- Ministry of Health Medical Device Manufacturing No. 005445
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
- Aug 24, 2016
- Expiry Date
- Aug 24, 2026
About this record
Access comprehensive regulatory information for GEZEN Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f6fca5f453c8ad4275f51d16050a3a4 and manufactured by BIOLIFE MEDICAL DEVICE INC.. The authorized representative in Taiwan is BIOLIFE MEDICAL DEVICE INC..
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