Taiwan FDA registration f7a8e5d8e246df923b2ddfdb481106b7

"Elifoss" Anaerobic Detection Media (Unsterilized)

TW: "艾利福斯"厭氧菌檢測培養基 (未滅菌)

Taiwan·Risk Class 1·Alifax S.r.l.·Registered Mar 15, 2019 – Mar 15, 2024Expired

Registration details

Analysis ID: f7a8e5d8e246df923b2ddfdb481106b7
Customs Code: DHA09402019207

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 15, 2019
Expiry Date: Mar 15, 2024

About this record

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..

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