Taiwan FDA registration 84366ec877624a1477c5d7cfb136a2af
“Zimmer” Nexel Total Elbow
TW: “捷邁”類骼手全人工肘關節
Taiwan·Risk Class 2·MD·ZIMMER INC.·Registered Mar 19, 2019 – Mar 19, 2029ActiveRegistration details
- Analysis ID
- 84366ec877624a1477c5d7cfb136a2af
- License Form
- Ministry of Health Medical Device Import No. 032337
- Customs Code
- DHA05603233703
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)
- N3150 Metal/metallic or metal/polymer cement compounds for restricted elbow joints
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 19, 2019
- Expiry Date
- Mar 19, 2029
About this record
Access comprehensive regulatory information for “Zimmer” Nexel Total Elbow in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84366ec877624a1477c5d7cfb136a2af and manufactured by ZIMMER INC.. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., LTD..
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