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"Fujifilm" airbag controller - Taiwan Registration dcc38b24c5324d4b7efe14ed7df84b07

Access comprehensive regulatory information for "Fujifilm" airbag controller in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number dcc38b24c5324d4b7efe14ed7df84b07 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. 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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dcc38b24c5324d4b7efe14ed7df84b07
Registration Details
Taiwan FDA Registration: dcc38b24c5324d4b7efe14ed7df84b07
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Device Details

"Fujifilm" airbag controller
TW: โ€œๅฏŒๅฃซโ€ๆฐฃๅ›ŠๆŽงๅˆถๅ™จ
Risk Class 2

Registration Details

dcc38b24c5324d4b7efe14ed7df84b07

DHA05603252109

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

Apr 22, 2019

Apr 22, 2029