“Collagen Matrix” DuraMend-Onlay Collagen Dura Substitute Membrane - Taiwan Registration 120e1d9ffb747c443913144585a29859
Access comprehensive regulatory information for “Collagen Matrix” DuraMend-Onlay Collagen Dura Substitute Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 120e1d9ffb747c443913144585a29859 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
120e1d9ffb747c443913144585a29859
Ministry of Health Medical Device Import No. 034144
DHA05603414402
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
Jan 04, 2021
Jan 04, 2026

