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“Arthrex” FiberTak suture anchor - Taiwan Registration 6d9008f08d5f1b934364b887f5ff458d

Access comprehensive regulatory information for “Arthrex” FiberTak suture anchor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6d9008f08d5f1b934364b887f5ff458d 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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6d9008f08d5f1b934364b887f5ff458d
Registration Details
Taiwan FDA Registration: 6d9008f08d5f1b934364b887f5ff458d
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Device Details

“Arthrex” FiberTak suture anchor
TW: “艾思瑞斯”凡博太克縫合錨釘
Risk Class 2
MD

Registration Details

6d9008f08d5f1b934364b887f5ff458d

Ministry of Health Medical Device Import No. 030021

DHA05603002105

Company Information

United States

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

Jul 25, 2017

Jul 25, 2027