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Alere Triage MeterPro (Non-Sterile) - Taiwan Registration 31eddd8f267c5d671048d5389f69bc76

Access comprehensive regulatory information for Alere Triage MeterPro (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 31eddd8f267c5d671048d5389f69bc76 and manufactured by ALERE SAN DIEGO, INC.. The authorized representative in Taiwan is BIO-CHECK LABORATORIES 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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31eddd8f267c5d671048d5389f69bc76
Registration Details
Taiwan FDA Registration: 31eddd8f267c5d671048d5389f69bc76
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Device Details

Alere Triage MeterPro (Non-Sterile)
TW: ็พŽ่‰พๅˆฉ็ˆพ ๆฃๆฅญ้ง’ ๅฐˆๅฎถๅž‹่žขๅ…‰ๅˆ†ๆžๅ„€ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

31eddd8f267c5d671048d5389f69bc76

Ministry of Health Medical Device Import Registration No. 006826

DHA08400682605

Company Information

United States

Product Details

Limited to the first-level identification range of the Measures for the Administration of Medical Devices "Fluorescence Instrument for Clinical Use (A.2560)".

A Clinical chemistry and clinical toxicology

A2560 fluorometer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023