Taiwan FDA registration da3ef03bce09bb2ee4234eca86f9b238

"BioMérieux" whitening separation Platelet aerobic flask (sterilized)

TW: “生物梅里埃”減白分離術血小板專用需氧培養瓶 (滅菌)

Taiwan·Risk Class 1·BIOMERIEUX, INC.·Registered Aug 01, 2013 – Aug 01, 2028Active

Registration details

Analysis ID: da3ef03bce09bb2ee4234eca86f9b238
Customs Code: DHA09401325106

Company information

Manufacturer: BIOMERIEUX, INC.
Manufacturer Country: United States
Authorized Representative: Hong Kong Commercial Mérieux S.p.A. Taiwan Branch

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: Aug 01, 2013
Expiry Date: Aug 01, 2028

About this record

Access comprehensive regulatory information for "BioMérieux" whitening separation Platelet aerobic flask (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number da3ef03bce09bb2ee4234eca86f9b238 and manufactured by BIOMERIEUX, INC.. The authorized representative in Taiwan is Hong Kong Commercial Mérieux S.p.A. Taiwan Branch.

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