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"Fujifilm" electronic digestive endoscope - Taiwan Registration 151197decc3c91243686353204467868

Access comprehensive regulatory information for "Fujifilm" electronic digestive endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 151197decc3c91243686353204467868 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Sano 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 2 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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151197decc3c91243686353204467868
Registration Details
Taiwan FDA Registration: 151197decc3c91243686353204467868
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Device Details

"Fujifilm" electronic digestive endoscope
TW: โ€œๅฏŒๅฃซโ€้›ปๅญๆถˆๅŒ–้“ๅ…ง่ฆ–้ก
Risk Class 2

Registration Details

151197decc3c91243686353204467868

DHA05603168801

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

Oct 22, 2018

Oct 22, 2028

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