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"ALIFAX" Microbiological specimen collection and transport device (Non-Sterile) - Taiwan Registration 5854e58f699854b52cf89ef3e80c50b3

Access comprehensive regulatory information for "ALIFAX" Microbiological specimen collection and transport 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 5854e58f699854b52cf89ef3e80c50b3 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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5854e58f699854b52cf89ef3e80c50b3
Registration Details
Taiwan FDA Registration: 5854e58f699854b52cf89ef3e80c50b3
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Device Details

"ALIFAX" Microbiological specimen collection and transport device (Non-Sterile)
TW: "่‰พๅˆฉ็ฆๆ–ฏ" ๅพฎ็”Ÿ็‰ฉๆจฃๆœฌๆ”ถ้›†ๅŠ่ผธ้€ๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

5854e58f699854b52cf89ef3e80c50b3

Ministry of Health Medical Device Import No. 019730

DHA09401973009

Company Information

Italy

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".

C Immunology and microbiology devices

C2900 Microbial sample collection and delivery device

Imported from abroad

Dates and Status

Oct 26, 2018

Oct 26, 2023