Taiwan FDA registration d33251ece93e7821c09a46338b110493

FENDIS Medical Patch (Unsterilized)

TW: 芬蒂思醫療用貼布 (未滅菌)

Taiwan·Risk Class 1·VENICE LABORATORIES CO., LTD.·Registered Jun 08, 2015 – Jun 08, 2025Expired

Registration details

Analysis ID: d33251ece93e7821c09a46338b110493

Company information

Manufacturer: VENICE LABORATORIES CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FANTASY INDUSTRY CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J.5240 Adhesive tapes and adhesive bandages for medical use
Import Information: Contract manufacturing;; Domestic

Dates and status

Registration Date: Jun 08, 2015
Expiry Date: Jun 08, 2025

About this record

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.