Taiwan FDA registration 655a2e5bf8774f19984d2fa3592ca380
"Difu" knee gama artificial femur knee joint system
TW: “帝富”膝格瑪人工股骨膝關節系統
Taiwan·Risk Class 2·DePuy Ireland UC;; DePuy Orthopaedics,Inc.·Registered Mar 15, 2011 – Mar 15, 2026ExpiredRegistration details
- Analysis ID
- 655a2e5bf8774f19984d2fa3592ca380
- Customs Code
- DHA00602222101
Company information
- Manufacturer
- DePuy Ireland UC;; DePuy Orthopaedics,Inc.
- Manufacturer Country
- Ireland;;United States
- 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
- Mar 15, 2011
- Expiry Date
- Mar 15, 2026
About this record
Access comprehensive regulatory information for "Difu" knee gama artificial femur 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 655a2e5bf8774f19984d2fa3592ca380 and manufactured by DePuy Ireland UC;; DePuy Orthopaedics,Inc.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..
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