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"Aitaka" Liquid Culture Base & Sampling Brush (Sterilization) - Taiwan Registration e308a1f91a80a80fb052eba0995728c3

Access comprehensive regulatory information for "Aitaka" Liquid Culture Base & Sampling Brush (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e308a1f91a80a80fb052eba0995728c3 and manufactured by Aptaca S.p.A.. The authorized representative in Taiwan is DiaTech Technology 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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e308a1f91a80a80fb052eba0995728c3
Registration Details
Taiwan FDA Registration: e308a1f91a80a80fb052eba0995728c3
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Device Details

"Aitaka" Liquid Culture Base & Sampling Brush (Sterilization)
TW: "่‰พๅก”ๅก" ๆถฒๆ…‹ๅŸน้คŠๅŸบๅŠๆŽกๆชขๅˆท (ๆป…่Œ)
Risk Class 1

Registration Details

e308a1f91a80a80fb052eba0995728c3

DHA09402336705

Company Information

Italy

Product Details

It is limited to the first-level identification scope of the "Enhanced Culture Medium (C.2330)" and "Microbial Sample Collection and Transportation Equipment (C.2900)" of the Measures for the Classification and Grading of Medical Devices.

C Immunology and microbiology

C.2330 ๅผทๅŒ–ๅŸน้คŠๅŸบ;; C.2900 ๅพฎ็”Ÿ็‰ฉๆจฃๆœฌๆ”ถ้›†ๅŠ่ผธ้€ๅ™จๆ

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Jan 16, 2024

Jan 16, 2029