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"ALIFAX" POSITIVE CONTROL KIT (Non-Sterile) - Taiwan Registration 4b1e029cbae5a8b44c258975f19744ca

Access comprehensive regulatory information for "ALIFAX" POSITIVE CONTROL KIT (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 4b1e029cbae5a8b44c258975f19744ca 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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4b1e029cbae5a8b44c258975f19744ca
Registration Details
Taiwan FDA Registration: 4b1e029cbae5a8b44c258975f19744ca
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Device Details

"ALIFAX" POSITIVE CONTROL KIT (Non-Sterile)
TW: "่‰พๅˆฉ็ฆๆ–ฏ"้™ฝๆ€งๅ“็ฎกๅฅ—็ต„(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4b1e029cbae5a8b44c258975f19744ca

Ministry of Health Medical Device Import No. 019871

DHA09401987101

Company Information

Italy

Product Details

Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A1660 Quality Control Materials (Analytical and Non-Analytical)

Imported from abroad

Dates and Status

Dec 03, 2018

Dec 03, 2023