Taiwan FDA registration 9cc82d63ec0eed8859c46c6008a09060
“SurFuse” Demineralized Bone Matrix
TW: “迅弗斯”去礦物質骨基質骨骼替代品
Taiwan·Risk Class 2·MD·HANS BIOMED CORP.·Registered May 26, 2016 – May 26, 2026ExpiredRegistration details
- Analysis ID
- 9cc82d63ec0eed8859c46c6008a09060
- License Form
- Ministry of Health Medical Device Import No. 028600
- Customs Code
- DHA05602860003
Company information
- Manufacturer
- HANS BIOMED CORP.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- A-SPINE Asia Co., Ltd.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- N Orthopedic devices
- Product Type (Level 2)
- N3045 Resorbed calcium salt bone cavity filling device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 26, 2016
- Expiry Date
- May 26, 2026
About this record
Access comprehensive regulatory information for “SurFuse” Demineralized Bone Matrix in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9cc82d63ec0eed8859c46c6008a09060 and manufactured by HANS BIOMED CORP.. The authorized representative in Taiwan is A-SPINE Asia Co., Ltd..
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