Taiwan FDA registration 72fd662e6ce3e267a14b44fb7ae46446
“Collagen Matrix” DuraMend Suturable Collagen Dura Membrane
TW: “凱力麥基”腦膜可縫合膠原膜
Taiwan·Risk Class 2·MD·Collagen Matrix Inc.·Registered Oct 29, 2020 – Oct 29, 2025ExpiredRegistration details
- Analysis ID
- 72fd662e6ce3e267a14b44fb7ae46446
- License Form
- Ministry of Health Medical Device Import No. 034011
- Customs Code
- DHA05603401109
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
- Oct 29, 2020
- Expiry Date
- Oct 29, 2025
About this record
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.
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