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"Fujifilm" front end fixing sleeve - Taiwan Registration a8e5c144053d72d5951ad0a4ecf0fa61

Access comprehensive regulatory information for "Fujifilm" front end fixing sleeve in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a8e5c144053d72d5951ad0a4ecf0fa61 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 3 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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a8e5c144053d72d5951ad0a4ecf0fa61
Registration Details
Taiwan FDA Registration: a8e5c144053d72d5951ad0a4ecf0fa61
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Device Details

"Fujifilm" front end fixing sleeve
TW: โ€œๅฏŒๅฃซโ€ๅ…ˆ็ซฏ้ƒจๅ›บๅฎšๅฅ—
Risk Class 2

Registration Details

a8e5c144053d72d5951ad0a4ecf0fa61

DHA05603299005

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

Nov 10, 2019

Nov 10, 2029

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