"Byken" absorbable collagen regeneration film
Taiwan·Risk Class 2·BICON, LLC·Registered Feb 25, 2011 – Feb 25, 2026Expired- Analysis ID
- 3f48c3e6530e84ae1e3a3668b2b20d26
- Customs Code
- DHA00602218102
- Manufacturer
- BICON, LLC
- Manufacturer Country
- United States
- Authorized Representative
- Taiwan Byken Co., Ltd
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dentistry
- Product Type (Level 2)
- F.3960 Inferior condyle supplement
- Import Information
- import
- Registration Date
- Feb 25, 2011
- Expiry Date
- Feb 25, 2026
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Access comprehensive regulatory information for "Byken" absorbable collagen regeneration film in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3f48c3e6530e84ae1e3a3668b2b20d26 and manufactured by BICON, LLC. The authorized representative in Taiwan is Taiwan Byken Co., Ltd.
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including BICON, LLC, and 1 recent registrations in the same category. 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.