Taiwan FDA registration 278f6dc2fee97d0bd59e85946c4b497c
P.F.C. Uni-Kenpamente Knee System
TW: Ｐ．Ｆ．Ｃ．尤尼－肯帕門特膝關節系統
Taiwan·JOHNSON & JOHNSON PROFESSIONAL INC.·Registered Dec 07, 1993 – Dec 07, 1998CancelledRegistration details
- Analysis ID
- 278f6dc2fee97d0bd59e85946c4b497c
- Customs Code
- DHA00600706306
Company information
- Manufacturer
- JOHNSON & JOHNSON PROFESSIONAL INC.
- Manufacturer Country
- United States
- Authorized Representative
- Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch
Product details
- Intended Use
- vacuum
- Product Type (Level 1)
- 0300 Prosthetic function substitute
- Import Information
- import
Dates and status
- Registration Date
- Dec 07, 1993
- Expiry Date
- Dec 07, 1998
- Cancellation Date
- Aug 24, 2000
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for P.F.C. Uni-Kenpamente Knee System in Taiwan's medical device market through Pure Global AI's free database. is registered under number 278f6dc2fee97d0bd59e85946c4b497c and manufactured by JOHNSON & JOHNSON PROFESSIONAL INC.. The authorized representative in Taiwan is Yingshang Zhuangsheng and Zhuangsheng (Hong Kong) Co., Ltd. Taiwan Branch.
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