Taiwan FDA registration f25bed8bfd9722614eee2f1729aa6865
“Collagen Matrix” DuraMend-Onlay Plus Collagen Dural Regeneration Matrix
TW: “凱力麥基”腦膜再生膠原基質
Taiwan·Risk Class 2·MD·COLLAGEN MATRIX, INC.·Registered Dec 31, 2020 – Dec 31, 2025ExpiredRegistration details
- Analysis ID
- f25bed8bfd9722614eee2f1729aa6865
- License Form
- Ministry of Health Medical Device Import No. 034138
- Customs Code
- DHA05603413807
Company information
- Manufacturer
- COLLAGEN MATRIX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- K Devices for neuroscience
- Product Type (Level 2)
- K5910 Hard Membrane Replacement
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 31, 2020
- Expiry Date
- Dec 31, 2025
About this record
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.
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