Taiwan FDA registration bd04fb75bb6448e5d1fd864f5c07c611

Thermo Fisher Scientific Adenovirus Antigen Fluorescence Test Kit (Unsterilized)

TW: "賽默飛世爾科技" 腺病毒抗原螢光檢驗試劑套組(未滅菌)

Taiwan·Risk Class 1·OXOID LIMITED;; Remel Europe Limited·Registered May 24, 2024 – May 24, 2029Active

Registration details

Analysis ID: bd04fb75bb6448e5d1fd864f5c07c611
Customs Code: DHA09402348501

Company information

Manufacturer: OXOID LIMITED;; Remel Europe Limited
Manufacturer Country: United Kingdom
Authorized Representative: THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.

Product details

Intended Use: It is limited to the first-level identification scope of the "Adenovirus Serum Reagent (C.3020)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1): C Immunology and microbiology
Product Type (Level 2): C.3020 腺病毒血清試劑
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: May 24, 2024
Expiry Date: May 24, 2029

About this record

Access comprehensive regulatory information for Thermo Fisher Scientific Adenovirus Antigen Fluorescence Test Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number bd04fb75bb6448e5d1fd864f5c07c611 and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..

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