Pure Global

Fujifilm Automatic Dry Biochemical Analyzer (Unsterilized) - Taiwan Registration 06a9a2135d4e12157ff856600fef06d1

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 06a9a2135d4e12157ff856600fef06d1 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Hanamaki Office. 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 IMAGING SYSTEMS (SUZHOU) CO., LTD., 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
3 Competitors
5 Recent Registrations
06a9a2135d4e12157ff856600fef06d1
Registration Details
Taiwan FDA Registration: 06a9a2135d4e12157ff856600fef06d1
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

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

Registration Details

06a9a2135d4e12157ff856600fef06d1

DHA08401900703

Company Information

Product Details

Limited to the first level identification range of the "Individual Photometric Chemistry Analyzer for Clinical Use (A.2160)" of the Measures for the Classification and Grading of Medical Devices.

A Clinical chemistry and clinical toxicology

A.2160 Individual Photometric Chemistry Analyzer for Clinical Use

Input;; QMS/QSD

Dates and Status

Oct 01, 2021

Oct 31, 2025