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FENDIS Medical Patch (Unsterilized) - Taiwan Registration d33251ece93e7821c09a46338b110493

Access comprehensive regulatory information for FENDIS Medical Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d33251ece93e7821c09a46338b110493 and manufactured by VENICE LABORATORIES CO., LTD.. The authorized representative in Taiwan is FANTASY INDUSTRY CO., LTD..

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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d33251ece93e7821c09a46338b110493
Registration Details
Taiwan FDA Registration: d33251ece93e7821c09a46338b110493
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Device Details

FENDIS Medical Patch (Unsterilized)
TW: ่Šฌ่’‚ๆ€ ้†ซ็™‚็”จ่ฒผๅธƒ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d33251ece93e7821c09a46338b110493

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification scope of the "Medical Adhesive Tapes and Adhesive Bandages (J.5240)" Classification and Grading Management Measures for Medical Equipment.

J General hospital and personal use equipment

J.5240 Adhesive tapes and adhesive bandages for medical use

Contract manufacturing;; Domestic

Dates and Status

Jun 08, 2015

Jun 08, 2025