Taiwan FDA registration 581490314f1a66006c291ed92aef9e52
"Ximei" Risia reconstructed ring and protective frame
TW: "西美" 里西雅重建環及護架
Registration details
- Analysis ID
- 581490314f1a66006c291ed92aef9e52
- Customs Code
- DHA00601024802
Company information
- Manufacturer
- ZIMMER INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Zimmer Medical Device Co., Ltd
Product details
- Product Type (Level 1)
- N Orthopedics
- Import Information
- import
Dates and status
- Registration Date
- Mar 19, 2003
- Expiry Date
- Mar 19, 2023
About this record
Access comprehensive regulatory information for "Ximei" Risia reconstructed ring and protective frame in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 581490314f1a66006c291ed92aef9e52 and manufactured by ZIMMER INC.. The authorized representative in Taiwan is Taiwan Zimmer Medical Device 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.
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