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“LIAISON” XL analyzer (Non-Sterile) - Taiwan Registration e57c3a323da6150b5bd4b9c320f39c9e

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 e57c3a323da6150b5bd4b9c320f39c9e and manufactured by DIASORIN S.P.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) 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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e57c3a323da6150b5bd4b9c320f39c9e
Registration Details
Taiwan FDA Registration: e57c3a323da6150b5bd4b9c320f39c9e
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Device Details

“LIAISON” XL analyzer (Non-Sterile)
TW: “禮亞尚” 全自動冷光免疫分析儀(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

e57c3a323da6150b5bd4b9c320f39c9e

Ministry of Health Medical Device Import No. 021801

DHA09402180101

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

Jul 30, 2020

Jul 30, 2025

Cancellation Information

Logged out

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