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"LIAISON" XL LAS Analyzer (Non-Sterile) - Taiwan Registration 4e6725401c6aab65423157430b68a88e

Access comprehensive regulatory information for "LIAISON" XL LAS 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 4e6725401c6aab65423157430b68a88e and manufactured by DIASORIN S.P.A.. 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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4e6725401c6aab65423157430b68a88e
Registration Details
Taiwan FDA Registration: 4e6725401c6aab65423157430b68a88e
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Device Details

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

Registration Details

4e6725401c6aab65423157430b68a88e

Ministry of Health Medical Device Import No. 020364

DHA09402036400

Company Information

Italy

Product Details

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad; GMP

Dates and Status

Apr 24, 2019

Apr 24, 2024

Cancellation Information

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