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"LIAISON" XL Analyzer (Non-Sterile) - Taiwan Registration bf202f983148ca7e1aa6851d8958063a

Access comprehensive regulatory information for "LIAISON" XL Analyzer (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bf202f983148ca7e1aa6851d8958063a and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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bf202f983148ca7e1aa6851d8958063a
Registration Details
Taiwan FDA Registration: bf202f983148ca7e1aa6851d8958063a
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Device Details

"LIAISON" XL Analyzer (Non-Sterile)
TW: "็ฆฎ้›…ๅฐš" ๅ…จ่‡ชๅ‹•ๅ†ทๅ…‰ๅ…็–ซๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

bf202f983148ca7e1aa6851d8958063a

Ministry of Health Medical Device Import No. 017573

DHA09401757309

Company Information

Germany

Product Details

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad; GMP

Dates and Status

Mar 08, 2017

Mar 08, 2022

Cancellation Information

Logged out

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