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"Elifoss" Microbial Identification and Determination Equipment (Unsterilized) - Taiwan Registration 59b8a20f65204e7d9a24adf884f64aa8

Access comprehensive regulatory information for "Elifoss" Microbial Identification and Determination Equipment (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 59b8a20f65204e7d9a24adf884f64aa8 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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59b8a20f65204e7d9a24adf884f64aa8
Registration Details
Taiwan FDA Registration: 59b8a20f65204e7d9a24adf884f64aa8
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Device Details

"Elifoss" Microbial Identification and Determination Equipment (Unsterilized)
TW: "่‰พๅˆฉ็ฆๆ–ฏ" ๅพฎ็”Ÿ็‰ฉ้‘‘ๅˆฅ่ˆ‡ๆธฌๅฎšๅ™จๆ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

59b8a20f65204e7d9a24adf884f64aa8

DHA09402196502

Company Information

Italy

Product Details

Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Microbial Identification and Determination Equipment (C.2660)".

C Immunology and microbiology

C.2660 ๅพฎ็”Ÿ็‰ฉ้‘‘ๅˆฅๅŠๆธฌๅฎšๅ™จๆ

Input;; QMS/QSD

Dates and Status

Sep 16, 2020

Sep 16, 2025