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"Byken" absorbable collagen regeneration film - Taiwan Registration fac48917744fe51ba849c2e95c505961

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 fac48917744fe51ba849c2e95c505961 and manufactured by BICON, LLC. The authorized representative in Taiwan is BICON TAIWAN 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.

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fac48917744fe51ba849c2e95c505961
Registration Details
Taiwan FDA Registration: fac48917744fe51ba849c2e95c505961
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Device Details

"Byken" absorbable collagen regeneration film
TW: โ€œๆ‹œ่‚ฏโ€ๅฏๅธๆ”ถๆ€ง่† ๅŽŸๅ†็”Ÿ่†œ
Risk Class 2

Registration Details

fac48917744fe51ba849c2e95c505961

DHA00602218102

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

F Dentistry

F.3960 Inferior condyle supplement

import

Dates and Status

Feb 25, 2011

Feb 25, 2026

Companies Making Similar Products
Top companies providing products similar to ""Byken" absorbable collagen regeneration film"

BICON, LLC

1 products

Latest registration: Feb 25, 2011

Recent Registrations
Recently registered similar products

"Byken" absorbable collagen regeneration film

Feb 25, 2011
Manufacturer:

BICON, LLC

Registration:

3f48c3e6530e84ae1e3a3668b2b20d26

Risk Class:

2