Taiwan FDA registration aeef81a3d78ac96c70284ecff8b1e300

Cyanidium typhi antigen test reagent (unsterilized)

TW: “速帝”傷寒沙門氏菌抗原檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·STANDARD DIAGNOSTICS, INC.·Registered Aug 12, 2010 – Aug 12, 2020Cancelled

Registration details

Analysis ID: aeef81a3d78ac96c70284ecff8b1e300
Customs Code: DHA04400908303

Company information

Manufacturer: STANDARD DIAGNOSTICS, INC.
Manufacturer Country: Korea, Republic of
Authorized Representative: Abbott Rapid Diagnostics Health Corp.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Salmonella Serological Reagent (C.3550)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3550 沙門氏菌屬血清試劑
Import Information: import

Dates and status

Registration Date: Aug 12, 2010
Expiry Date: Aug 12, 2020
Cancellation Date: Jul 15, 2022

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for Cyanidium typhi antigen test reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number aeef81a3d78ac96c70284ecff8b1e300 and manufactured by STANDARD DIAGNOSTICS, INC.. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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