Taiwan FDA registration e308a1f91a80a80fb052eba0995728c3

"Aitaka" Liquid Culture Base & Sampling Brush (Sterilization)

TW: "艾塔卡" 液態培養基及採檢刷 (滅菌)

Taiwan·Risk Class 1·Aptaca S.p.A.·Registered Jan 16, 2024 – Jan 16, 2029Active

Registration details

Analysis ID: e308a1f91a80a80fb052eba0995728c3
Customs Code: DHA09402336705

Company information

Manufacturer: Aptaca S.p.A.
Manufacturer Country: Italy
Authorized Representative: DiaTech Technology Co., Ltd.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2330 強化培養基;; C.2900 微生物樣本收集及輸送器材
Import Information: QMS/QSD;; 輸入

Dates and status

Registration Date: Jan 16, 2024
Expiry Date: Jan 16, 2029

About this record

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..

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