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"Medical Complete" UTAS and Light i30 Individual Photometric Chemistry Analyzer (Unsterilized) - Taiwan Registration d3d2e1d18789fbe489e3e81e97abb087

Access comprehensive regulatory information for "Medical Complete" UTAS and Light i30 Individual Photometric Chemistry 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 d3d2e1d18789fbe489e3e81e97abb087 and manufactured by FUJIFILM Healthcare Manufacturing Corporation Minamiashigara Takematsu Office;; FUJIFILM WAKO PURE CHEMICAL CORPORATION. The authorized representative in Taiwan is MEDICARE PRODUCTS INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FUJIFILM TECHNO PRODUCTS CO., LTD. TAKEMATSU FACTORY;; FUJIFILM WAKO PURE CHEMICAL CORPORATION, and 1 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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d3d2e1d18789fbe489e3e81e97abb087
Registration Details
Taiwan FDA Registration: d3d2e1d18789fbe489e3e81e97abb087
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Device Details

"Medical Complete" UTAS and Light i30 Individual Photometric Chemistry Analyzer (Unsterilized)
TW: "้†ซๅ…จ" ๅ„ชๅก”ๆ–ฏๅ’Œๅ…‰i30ๅ€‹ๅˆฅๅผๅ…‰ๅบฆ้‡ๆธฌๅŒ–ๅญธๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d3d2e1d18789fbe489e3e81e97abb087

DHA08401554501

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

QMS/QSD;; ๅง”่จ—่ฃฝ้€ ;; ่ผธๅ…ฅ

Dates and Status

Oct 01, 2021

Oct 31, 2025

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