Taiwan FDA registration d7930f906c3265069b33456e8cb12cc1

"FUJIFILM" Gastroenterology-urology biopsy instrument (Non-Sterile)

TW: "富士" 腸胃科-泌尿科生檢器械 (未滅菌)

Taiwan·Risk Class 1·MD·FUJIFILM CORPORATION·Registered Apr 26, 2016 – Apr 26, 2021Expired

Registration details

Analysis ID: d7930f906c3265069b33456e8cb12cc1
License Form: Ministry of Health Medical Device Import No. 016449
Customs Code: DHA09401644903

Company information

Manufacturer: FUJIFILM CORPORATION
Manufacturer Country: Japan
Authorized Representative: WELMORE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Gastroenterology-Urology Bioexamination Devices (H.1075)".
Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H1075 Gastroenterology - Urology biopsy instruments
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 26, 2016
Expiry Date: Apr 26, 2021

About this record

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..

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