Taiwan FDA registration 9997ca02d36aa30b8546361b41a872ba

“Fortune” FixPad Anchoring Device (Non-Sterile)

TW: “富強” 導管固定貼(未滅菌)

Taiwan·Risk Class 1·MD·FORTUNE MEDICAL INSTRUMENT CORP.·Registered Jul 07, 2020 – Jul 07, 2025Expired

Registration details

Analysis ID: 9997ca02d36aa30b8546361b41a872ba
License Form: Ministry of Health Medical Device Manufacturing No. 008423

Company information

Manufacturer: FORTUNE MEDICAL INSTRUMENT CORP.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: FORTUNE MEDICAL INSTRUMENT CORP.

Product details

Intended Use: 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)".
Product Type (Level 1): J General hospital and personal use equipment
Product Type (Level 2): J5240 Medical adhesive tapes and adhesive bandages
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Jul 07, 2020
Expiry Date: Jul 07, 2025

About this record

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.