Taiwan FDA registration 2f5b47c05d6cc7eef8283d7c42f65c34
Artificial repair rod
TW: 人工修補棒
Taiwan·MANUFACTURED BY BIOSIL LTD.·Registered Sep 14, 1995 – Feb 09, 2004CancelledRegistration details
- Analysis ID
- 2f5b47c05d6cc7eef8283d7c42f65c34
- Customs Code
- DHA00600762203
Company information
- Manufacturer
- MANUFACTURED BY BIOSIL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- Sangang Enterprise Co., Ltd
Product details
- Product Type (Level 1)
- 0399 Other artificial function substitutes
- Import Information
- import
Dates and status
- Registration Date
- Sep 14, 1995
- Expiry Date
- Feb 09, 2004
- Cancellation Date
- Jul 30, 2007
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Artificial repair rod in Taiwan's medical device market through Pure Global AI's free database. is registered under number 2f5b47c05d6cc7eef8283d7c42f65c34 and manufactured by MANUFACTURED BY BIOSIL LTD.. The authorized representative in Taiwan is Sangang Enterprise 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