Taiwan FDA registration c1bc35478ad5b50147c63092492978ef
“Zimmer” NexGen Complete Knee Solution Augments
TW: “捷邁”新世紀人工膝關節墊塊
Taiwan·Risk Class 2·MD·ZIMMER, INC.·Registered Oct 10, 2019 – Oct 10, 2024ExpiredRegistration details
- Analysis ID
- c1bc35478ad5b50147c63092492978ef
- License Form
- Ministry of Health Medical Device Import No. 032865
- Customs Code
- DHA05603286502
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
- Oct 10, 2019
- Expiry Date
- Oct 10, 2024
About this record
Access comprehensive regulatory information for “Zimmer” NexGen Complete Knee Solution Augments in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c1bc35478ad5b50147c63092492978ef and manufactured by ZIMMER, INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., 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