Taiwan FDA registration 702d42cfb42ad1aa3c1ad363a492a973
“Collagen Matrix” NuOss Anorganic Bovine Bone
TW: “凱樂基”紐歐斯骨粉
Taiwan·Risk Class 2·MD·COLLAGEN MATRIX, INC.·Registered Mar 22, 2018 – Mar 22, 2028ActiveRegistration details
- Analysis ID
- 702d42cfb42ad1aa3c1ad363a492a973
- License Form
- Ministry of Health Medical Device Import No. 030990
- Customs Code
- DHA05603099008
Company information
- Manufacturer
- COLLAGEN MATRIX, INC.
- Manufacturer Country
- United States
- Authorized Representative
- HUNG KUO MEDICAL INSTRUMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- F Dental devices
- Product Type (Level 2)
- F3930 Alveolar Restoration Materials
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 22, 2018
- Expiry Date
- Mar 22, 2028
About this record
Access comprehensive regulatory information for “Collagen Matrix” NuOss Anorganic Bovine Bone in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 702d42cfb42ad1aa3c1ad363a492a973 and manufactured by COLLAGEN MATRIX, INC.. The authorized representative in Taiwan is HUNG KUO MEDICAL INSTRUMENT CO., LTD..
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