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Fujifilm New Automatic Dry Biochemical Analyzer (Unsterilized) - Taiwan Registration 124b06745162ba35b9d423a358aaacdc

Access comprehensive regulatory information for Fujifilm New 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 124b06745162ba35b9d423a358aaacdc and manufactured by FUJIFILM TECHNO PRODUCTS CO., LTD. TOHOKU FACTORY HANAMAKI SITE. The authorized representative in Taiwan is HUNG CHONG CORP..

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124b06745162ba35b9d423a358aaacdc
Registration Details
Taiwan FDA Registration: 124b06745162ba35b9d423a358aaacdc
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Device Details

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

Registration Details

124b06745162ba35b9d423a358aaacdc

DHA04400638007

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

import

Dates and Status

Dec 12, 2007

Dec 12, 2017

Dec 13, 2019

Cancellation Information

Logged out

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