Taiwan FDA registration 8a28c3df74689fe94a743da99342045d

"Elifoss" Automated Media Kit (Unsterilized)

TW: "艾利福斯" 自動化培養基套組 (未滅菌)

Taiwan·Risk Class 1·Alifax S.r.l.·Registered Mar 07, 2019 – Mar 07, 2024Expired

Registration details

Analysis ID: 8a28c3df74689fe94a743da99342045d
Customs Code: DHA09402014906

Company information

Manufacturer: Alifax S.r.l.
Manufacturer Country: Italy
Authorized Representative: GRAND MARQUIS CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.2560 Microbial growth monitors
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Mar 07, 2019
Expiry Date: Mar 07, 2024

About this record

Access comprehensive regulatory information for "Elifoss" Automated Media Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8a28c3df74689fe94a743da99342045d and manufactured by Alifax S.r.l.. The authorized representative in Taiwan is GRAND MARQUIS CO., LTD..

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