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“Arthrex” Camera Head - Taiwan Registration 757fcf2db637822a48dbd2d299aa9f38

Access comprehensive regulatory information for “Arthrex” Camera Head in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 757fcf2db637822a48dbd2d299aa9f38 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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757fcf2db637822a48dbd2d299aa9f38
Registration Details
Taiwan FDA Registration: 757fcf2db637822a48dbd2d299aa9f38
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Device Details

“Arthrex” Camera Head
TW: “艾思瑞斯”攝影頭
Risk Class 2
MD

Registration Details

757fcf2db637822a48dbd2d299aa9f38

Ministry of Health Medical Device Import No. 030557

DHA05603055707

Company Information

United States

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Nov 16, 2017

Nov 16, 2022