“Collagen Matrix” DuraMend-Onlay Plus Collagen Dural Regeneration Matrix - Taiwan Registration f25bed8bfd9722614eee2f1729aa6865
Access comprehensive regulatory information for “Collagen Matrix” DuraMend-Onlay Plus Collagen Dural Regeneration Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f25bed8bfd9722614eee2f1729aa6865 and manufactured by COLLAGEN MATRIX, INC.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.
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.
Device Details
Registration Details
f25bed8bfd9722614eee2f1729aa6865
Ministry of Health Medical Device Import No. 034138
DHA05603413807
Product Details
For details, it is Chinese approved copy of the imitation order
K Devices for neuroscience
K5910 Hard Membrane Replacement
Imported from abroad
Dates and Status
Dec 31, 2020
Dec 31, 2025

