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Flushing equipment and accessories for Fujifilm endoscopes - Taiwan Registration d72e53657a363dfbeb6c3582523cf7c0

Access comprehensive regulatory information for Flushing equipment and accessories for Fujifilm endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d72e53657a363dfbeb6c3582523cf7c0 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki 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 Hanamaki 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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d72e53657a363dfbeb6c3582523cf7c0
Registration Details
Taiwan FDA Registration: d72e53657a363dfbeb6c3582523cf7c0
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Device Details

Flushing equipment and accessories for Fujifilm endoscopes
TW: โ€œๅฏŒๅฃซโ€ๅ…ง่ฆ–้ก็”จๆฒ–ๆฐด่จญๅ‚™ๅŠ้™„ไปถ
Risk Class 2

Registration Details

d72e53657a363dfbeb6c3582523cf7c0

DHA05603611900

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

Dec 02, 2022

Dec 02, 2027

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