Pure Global

“Arthrex” SutureTak Suture Anchor - Taiwan Registration 7489780c2ce8f4e0b9df5c40fd27289b

Access comprehensive regulatory information for “Arthrex” SutureTak 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 7489780c2ce8f4e0b9df5c40fd27289b 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
7489780c2ce8f4e0b9df5c40fd27289b
Registration Details
Taiwan FDA Registration: 7489780c2ce8f4e0b9df5c40fd27289b
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

“Arthrex” SutureTak Suture Anchor
TW: “艾思瑞斯”思求太克縫合錨釘
Risk Class 2
MD

Registration Details

7489780c2ce8f4e0b9df5c40fd27289b

Ministry of Health Medical Device Import No. 029649

DHA05602964902

Company Information

United States

Product Details

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

N Orthopedic devices

N3030 Single or multi-metal bone fixation device and accessories

Imported from abroad

Dates and Status

Apr 25, 2017

Apr 25, 2027