Taiwan FDA registration bd5189f301914dc2c5a2fa6122ccaa9b
“Zimmer” Persona Revision Knee System
TW: “捷邁” 博適耐重建型全人工膝關節系統
Taiwan·Risk Class 2·MD·ZIMMER, INC.·Registered Oct 07, 2022 – Oct 07, 2027ActiveRegistration details
- Analysis ID
- bd5189f301914dc2c5a2fa6122ccaa9b
- License Form
- Ministry of Health Medical Device Import No. 035929
- Customs Code
- DHA05603592904
Company information
- Manufacturer
- ZIMMER, INC.
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- N Orthopedics
- Product Type (Level 2)
- N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 07, 2022
- Expiry Date
- Oct 07, 2027
About this record
Access comprehensive regulatory information for “Zimmer” Persona Revision Knee System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bd5189f301914dc2c5a2fa6122ccaa9b and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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