Taiwan FDA registration 62052cfb63cafcba6137f8cb9489196c
"Difu" full artificial knee joint system
TW: "帝富"全人工膝關節系統
Taiwan·Risk Class 2·DEPUY INTERNATIONAL LTD.·Registered Sep 21, 2006 – Sep 21, 2021CancelledRegistration details
- Analysis ID
- 62052cfb63cafcba6137f8cb9489196c
- Customs Code
- DHA00601714106
Company information
- Manufacturer
- DEPUY INTERNATIONAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
- Import Information
- import
Dates and status
- Registration Date
- Sep 21, 2006
- Expiry Date
- Sep 21, 2021
- Cancellation Date
- Nov 02, 2018
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for "Difu" full artificial knee joint system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 62052cfb63cafcba6137f8cb9489196c and manufactured by DEPUY INTERNATIONAL LTD.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices