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Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) - Taiwan Registration af875f933410e4a4c3ffe5b65295e62c

Access comprehensive regulatory information for Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number af875f933410e4a4c3ffe5b65295e62c and manufactured by FUJIFILM IMAGING SYSTEMS (SUZHOU) CO., LTD.. The authorized representative in Taiwan is HUNG CHONG CORP..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE, FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office, and 5 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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af875f933410e4a4c3ffe5b65295e62c
Registration Details
Taiwan FDA Registration: af875f933410e4a4c3ffe5b65295e62c
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Device Details

Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized)
TW: โ€œๅฏŒๅฃซโ€ๅ…จ่‡ชๅ‹•ไนพๅผ็”ŸๅŒ–ๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

af875f933410e4a4c3ffe5b65295e62c

DHA04600192807

Company Information

Product Details

Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2160 Individual Photometric Chemistry Analyzer for Clinical Use

Chinese goods;; Input;; QMS/QSD

Dates and Status

Jul 08, 2013

Jul 08, 2018

Jul 15, 2022

Cancellation Information

Logged out

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