"FUJIFILM" Gastroenterology-urology biopsy instrument (Non-Sterile) - Taiwan Registration d7930f906c3265069b33456e8cb12cc1
Access comprehensive regulatory information for "FUJIFILM" Gastroenterology-urology biopsy instrument (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 d7930f906c3265069b33456e8cb12cc1 and manufactured by FUJIFILM CORPORATION. The authorized representative in Taiwan is WELMORE 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.
Device Details
Registration Details
d7930f906c3265069b33456e8cb12cc1
Ministry of Health Medical Device Import No. 016449
DHA09401644903
Product Details
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Gastroenterology-Urology Bioexamination Devices (H.1075)".
H Gastroenterology-urology devices
H1075 Gastroenterology - Urology biopsy instruments
Imported from abroad
Dates and Status
Apr 26, 2016
Apr 26, 2021