Pure Global

“Collagen Matrix” DuraMend Suturable Collagen Dura Membrane - Taiwan Registration 72fd662e6ce3e267a14b44fb7ae46446

Access comprehensive regulatory information for “Collagen Matrix” DuraMend Suturable Collagen Dura Membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 72fd662e6ce3e267a14b44fb7ae46446 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
72fd662e6ce3e267a14b44fb7ae46446
Registration Details
Taiwan FDA Registration: 72fd662e6ce3e267a14b44fb7ae46446
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Collagen Matrix” DuraMend Suturable Collagen Dura Membrane
TW: “凱力麥基”腦膜可縫合膠原膜
Risk Class 2
MD

Registration Details

72fd662e6ce3e267a14b44fb7ae46446

Ministry of Health Medical Device Import No. 034011

DHA05603401109

Company Information

United States

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

Oct 29, 2020

Oct 29, 2025