Taiwan FDA registration 15c5a8bee5939d3f43f43ae63d2f64aa
"Western American" reconstructed bone plate system
TW: "西美"重建型骨板系統
Registration details
- Analysis ID
- 15c5a8bee5939d3f43f43ae63d2f64aa
- Customs Code
- DHA00600945000
Company information
- Manufacturer
- ZIMMER INC.
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Zimmer Medical Device Co., Ltd
Product details
- Product Type (Level 1)
- 9999 Other
- Import Information
- import
Dates and status
- Registration Date
- Jul 07, 2000
- Expiry Date
- Jul 07, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Western American" reconstructed bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 15c5a8bee5939d3f43f43ae63d2f64aa 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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