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“Fortune” FixPad Anchoring Device (Non-Sterile) - Taiwan Registration 9997ca02d36aa30b8546361b41a872ba

Access comprehensive regulatory information for “Fortune” FixPad Anchoring Device (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9997ca02d36aa30b8546361b41a872ba and manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. The authorized representative in Taiwan is FORTUNE MEDICAL INSTRUMENT CORP..

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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9997ca02d36aa30b8546361b41a872ba
Registration Details
Taiwan FDA Registration: 9997ca02d36aa30b8546361b41a872ba
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Device Details

“Fortune” FixPad Anchoring Device (Non-Sterile)
TW: “富強” 導管固定貼(未滅菌)
Risk Class 1
MD

Registration Details

9997ca02d36aa30b8546361b41a872ba

Ministry of Health Medical Device Manufacturing No. 008423

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Adhesive Tapes and Adhesive Bandages for Medical Use (J.5240)".

J General hospital and personal use equipment

J5240 Medical adhesive tapes and adhesive bandages

Produced in Taiwan, China

Dates and Status

Jul 07, 2020

Jul 07, 2025