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“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.

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f25bed8bfd9722614eee2f1729aa6865
Registration Details
Taiwan FDA Registration: f25bed8bfd9722614eee2f1729aa6865
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Device Details

“Collagen Matrix” DuraMend-Onlay Plus Collagen Dural Regeneration Matrix
TW: “凱力麥基”腦膜再生膠原基質
Risk Class 2
MD

Registration Details

f25bed8bfd9722614eee2f1729aa6865

Ministry of Health Medical Device Import No. 034138

DHA05603413807

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

Dec 31, 2020

Dec 31, 2025