Taiwan FDA registration 27cf5e1da9294cf767d8cfd83f08c57a
“Zimmer” NexGen Prolong Highly Crosslinked Polyethylene Inset All Poly Patella
TW: “捷邁”新世紀高分子聚乙烯人工膝關節用髕骨
Taiwan·Risk Class 2·MD·ZIMMER,INC.·Registered Dec 25, 2013 – Dec 25, 2028ActiveRegistration details
- Analysis ID
- 27cf5e1da9294cf767d8cfd83f08c57a
- License Form
- Ministry of Health Medical Device Import No. 025742
- Customs Code
- DHA05602574208
Company information
- Manufacturer
- ZIMMER,INC.
- Manufacturer Country
- United States
- Authorized Representative
- ZIMMER BIOMET TAIWAN CO., LTD.
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)
- N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 25, 2013
- Expiry Date
- Dec 25, 2028
About this record
Access comprehensive regulatory information for “Zimmer” NexGen Prolong Highly Crosslinked Polyethylene Inset All Poly Patella in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 27cf5e1da9294cf767d8cfd83f08c57a and manufactured by ZIMMER,INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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