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“Arthrex” SpeedCinch - Taiwan Registration b88a5c733e96cb18ecb45068acc6d729

Access comprehensive regulatory information for “Arthrex” SpeedCinch in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b88a5c733e96cb18ecb45068acc6d729 and manufactured by Arthrex Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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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b88a5c733e96cb18ecb45068acc6d729
Registration Details
Taiwan FDA Registration: b88a5c733e96cb18ecb45068acc6d729
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Device Details

“Arthrex” SpeedCinch
TW: “艾思瑞斯”半月軟骨縫合修補器
Risk Class 2
MD

Registration Details

b88a5c733e96cb18ecb45068acc6d729

Ministry of Health Medical Device Import No. 029627

DHA05602962702

Company Information

United States

Product Details

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

I General and plastic surgical devices

I5000 Non-absorbable polyethylene suture

Imported from abroad

Dates and Status

Apr 12, 2017

Apr 12, 2022