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Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) - Taiwan Registration 39221fcc168208350f7f3181db872356

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 39221fcc168208350f7f3181db872356 and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..

This page provides complete technical specifications, regulatory compliance details, 3 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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39221fcc168208350f7f3181db872356
Registration Details
Taiwan FDA Registration: 39221fcc168208350f7f3181db872356
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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

39221fcc168208350f7f3181db872356

DHA04401187209

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

Input;; QMS/QSD

Dates and Status

Jun 26, 2012

Jun 26, 2017

Dec 13, 2019

Cancellation Information

Logged out

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