Taiwan FDA registration 4d72344e11118606b70e0eafbc2a8cb0

"Abbot" adenovirus antigen rapid test reagent (unsterilized)

TW: “亞培”腺病毒抗原快速檢測試劑(未滅菌)

Taiwan·Risk Class 1·ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT·Registered Jan 11, 2012 – Jan 11, 2022Cancelled

Registration details

Analysis ID: 4d72344e11118606b70e0eafbc2a8cb0
Customs Code: DHA04401128800

Company information

Manufacturer: ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT
Manufacturer Country: Japan
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 "Adenovirus Serological Reagent (C.3020)".
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑
Import Information: import

Dates and status

Registration Date: Jan 11, 2012
Expiry Date: Jan 11, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Abbot" adenovirus antigen 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 4d72344e11118606b70e0eafbc2a8cb0 and manufactured by ABBOTT DIAGNOSTICS MEDICAL CO., LTD.-CHIBA PLANT. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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