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"Elifoss" Anaerobic Detection Media (Unsterilized) - Taiwan Registration f7a8e5d8e246df923b2ddfdb481106b7

Access comprehensive regulatory information for "Elifoss" Anaerobic Detection Media (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f7a8e5d8e246df923b2ddfdb481106b7 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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f7a8e5d8e246df923b2ddfdb481106b7
Registration Details
Taiwan FDA Registration: f7a8e5d8e246df923b2ddfdb481106b7
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Device Details

"Elifoss" Anaerobic Detection Media (Unsterilized)
TW: "่‰พๅˆฉ็ฆๆ–ฏ"ๅŽญๆฐง่ŒๆชขๆธฌๅŸน้คŠๅŸบ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

f7a8e5d8e246df923b2ddfdb481106b7

DHA09402019207

Company Information

Italy

Product Details

It is limited to the first level of identification scope of the microbial growth monitor (C.2560) of the management measures for the classification and grading of medical devices.

C Immunology and microbiology

C.2560 Microbial growth monitors

Input;; QMS/QSD

Dates and Status

Mar 15, 2019

Mar 15, 2024