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"ALIFAX" Microtiter diluting and dispensing device (Non-sterile) - Taiwan Registration 39a6b0ec37be77d2970536e276a656d8

Access comprehensive regulatory information for "ALIFAX" Microtiter diluting and dispensing device (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 39a6b0ec37be77d2970536e276a656d8 and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS 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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39a6b0ec37be77d2970536e276a656d8
Registration Details
Taiwan FDA Registration: 39a6b0ec37be77d2970536e276a656d8
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Device Details

"ALIFAX" Microtiter diluting and dispensing device (Non-sterile)
TW: "่‰พๅˆฉ็ฆๆ–ฏ" ๅพฎๆปดๅฎš็จ€้‡‹ๅŠๅˆ†้…ๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

39a6b0ec37be77d2970536e276a656d8

Ministry of Health Medical Device Import No. 020289

DHA09402028909

Company Information

Italy

Product Details

Limited to the first level identification range of microtitration dilution and dispensing equipment (C.2500) of the management measures for medical devices.

C Immunology and microbiology devices

C2500 Microtitration Dilution and Dispensing Equipment

Imported from abroad

Dates and Status

Apr 10, 2019

Apr 10, 2024