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“Smith & Nephew” BICEPTOR BIOSURE PK Screw Kit - Taiwan Registration accabba1ce390ffec6aeffaaf3d0abb2

Access comprehensive regulatory information for “Smith & Nephew” BICEPTOR BIOSURE PK Screw Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number accabba1ce390ffec6aeffaaf3d0abb2 and manufactured by SMITH & NEPHEW, INC., ENDOSCOPY DIVISION. The authorized representative in Taiwan is SMITH & NEPHEW ( OVERSEAS ) LIMITED, TAIWAN BRANCH (U.K.).

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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accabba1ce390ffec6aeffaaf3d0abb2
Registration Details
Taiwan FDA Registration: accabba1ce390ffec6aeffaaf3d0abb2
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Device Details

“Smith & Nephew” BICEPTOR BIOSURE PK Screw Kit
TW: “史耐輝”不可吸收固定螺釘套組
Risk Class 2
MD

Registration Details

accabba1ce390ffec6aeffaaf3d0abb2

Ministry of Health Medical Device Import No. 034121

DHA05603412103

Company Information

Product Details

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

N Orthopedic devices

N3040 Smooth or threaded metal bone fixation

Imported from abroad

Dates and Status

Dec 10, 2020

Dec 10, 2025