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“SurFuse” Demineralized Bone Matrix - Taiwan Registration 9cc82d63ec0eed8859c46c6008a09060

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..

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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9cc82d63ec0eed8859c46c6008a09060
Registration Details
Taiwan FDA Registration: 9cc82d63ec0eed8859c46c6008a09060
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Device Details

“SurFuse” Demineralized Bone Matrix
TW: “迅弗斯”去礦物質骨基質骨骼替代品
Risk Class 2
MD

Registration Details

9cc82d63ec0eed8859c46c6008a09060

Ministry of Health Medical Device Import No. 028600

DHA05602860003

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Imported from abroad

Dates and Status

May 26, 2016

May 26, 2026