Taiwan FDA registration 59157f6987a2353c99a943101039afab

Abbot's Rotavirus/Adenovirus Rapid Test (Unsterilized)

TW: “亞培”輪狀病毒/腺病毒快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·ABBOTT DIAGNOSTICS KOREA INC·Registered Aug 12, 2010 – Aug 12, 2025Expired

Registration details

Analysis ID: 59157f6987a2353c99a943101039afab
Customs Code: DHA04400907708

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 "Adenovirus Serum Reagent (C.3020)" and "Poliovirus Serum Reagent (C.3405)" of the Classification and Grading Management Measures for Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑;; C.3405 小兒麻痺病毒血清試劑
Import Information: import

Dates and status

Registration Date: Aug 12, 2010
Expiry Date: Aug 12, 2025

About this record

Access comprehensive regulatory information for Abbot's Rotavirus/Adenovirus Rapid Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 59157f6987a2353c99a943101039afab and manufactured by ABBOTT DIAGNOSTICS KOREA INC. The authorized representative in Taiwan is Abbott Rapid Diagnostics Health Corp..

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