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"Fujifilm" ultrasound endoscope airbag - Taiwan Registration 2347549fed7dd5ba5a0805048998fe1b

Access comprehensive regulatory information for "Fujifilm" ultrasound endoscope airbag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2347549fed7dd5ba5a0805048998fe1b 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 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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2347549fed7dd5ba5a0805048998fe1b
Registration Details
Taiwan FDA Registration: 2347549fed7dd5ba5a0805048998fe1b
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Device Details

"Fujifilm" ultrasound endoscope airbag
TW: โ€œๅฏŒๅฃซโ€่ถ…้Ÿณๆณขๅ…ง่ฆ–้ก็”จๆฐฃๅ›Š
Risk Class 2

Registration Details

2347549fed7dd5ba5a0805048998fe1b

DHA05603529209

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

Mar 11, 2022

Mar 11, 2027

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