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“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.

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120e1d9ffb747c443913144585a29859
Registration Details
Taiwan FDA Registration: 120e1d9ffb747c443913144585a29859
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Device Details

“Collagen Matrix” DuraMend-Onlay Collagen Dura Substitute Membrane
TW: “凱力麥基”腦膜防護膠原膜
Risk Class 2
MD

Registration Details

120e1d9ffb747c443913144585a29859

Ministry of Health Medical Device Import No. 034144

DHA05603414402

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

Jan 04, 2021

Jan 04, 2026