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"Fujifilm" ultrasound gastroscope - Taiwan Registration 05fe6e048073d5bd480994dd7cc23ab8

Access comprehensive regulatory information for "Fujifilm" ultrasound gastroscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05fe6e048073d5bd480994dd7cc23ab8 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hitachiomiya Office;; FUJIFILM CORPORATION. The authorized representative in Taiwan is FUJIFILM HEALTHCARE TAIWAN CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM Healthcare Manufacturing Corporation Sano Office;; FUJIFILM CORPORATION, and 1 recent registrations in the same category. 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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05fe6e048073d5bd480994dd7cc23ab8
Registration Details
Taiwan FDA Registration: 05fe6e048073d5bd480994dd7cc23ab8
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Device Details

"Fujifilm" ultrasound gastroscope
TW: โ€œๅฏŒๅฃซโ€่ถ…้Ÿณๆณข่…ธ่ƒƒ้ก
Risk Class 2

Registration Details

05fe6e048073d5bd480994dd7cc23ab8

DHA00602315302

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Jan 04, 2012

Jan 04, 2027

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