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Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) - Taiwan Registration 51244f20e5c7227dde876eedee4d7b42

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 51244f20e5c7227dde876eedee4d7b42 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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51244f20e5c7227dde876eedee4d7b42
Registration Details
Taiwan FDA Registration: 51244f20e5c7227dde876eedee4d7b42
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Device Details

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

Registration Details

51244f20e5c7227dde876eedee4d7b42

DHA09401900702

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

Apr 25, 2018

Apr 25, 2023

Sep 30, 2021

Cancellation Information

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