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"Fujifilm" front end fixing sleeve - Taiwan Registration 2fe822feeaafc73b0937bb492ac5cf17

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 2fe822feeaafc73b0937bb492ac5cf17 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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2fe822feeaafc73b0937bb492ac5cf17
Registration Details
Taiwan FDA Registration: 2fe822feeaafc73b0937bb492ac5cf17
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Device Details

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

Registration Details

2fe822feeaafc73b0937bb492ac5cf17

DHA05603469908

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Jul 11, 2021

Jul 11, 2026

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