Taiwan FDA registration 1ea025278b0665859d8ae450cdca26f4

"Abbott" Typhimurium antibody rapid test reagent (unsterilized)

TW: “亞培”百而靈傷寒沙門氏菌抗體快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·ABBOTT DIAGNOSTICS KOREA INC·Registered Feb 11, 2015 – Feb 11, 2030Active

Registration details

Analysis ID: 1ea025278b0665859d8ae450cdca26f4
Customs Code: DHA09401491509

Company information

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

Product details

Intended Use: It is limited to the first-level identification scope of the "Salmonella Serum Reagent (C.3550)" of the Measures for the Classification and Grading of Medical Devices.
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: Feb 11, 2015
Expiry Date: Feb 11, 2030

About this record

Access comprehensive regulatory information for "Abbott" Typhimurium antibody rapid 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 1ea025278b0665859d8ae450cdca26f4 and manufactured by ABBOTT DIAGNOSTICS KOREA INC. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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