Taiwan FDA registration ba7b90ad477cd50b316c41447113b738
"Thermo Flying Technologies" Influenza A & B Antigen Ray Test Kit (Uninanished)
TW: "賽默飛世爾科技" A 和 B 型流感病毒抗原螢光檢驗試劑套組(未滅菌)
Registration details
- Analysis ID
- ba7b90ad477cd50b316c41447113b738
- Customs Code
- DHA09402348205
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 influenza virus serum reagent (C.3330) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3330 流感病毒血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- May 23, 2024
- Expiry Date
- May 23, 2029
About this record
Access comprehensive regulatory information for "Thermo Flying Technologies" Influenza A & B Antigen Ray Test Kit (Uninanished) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ba7b90ad477cd50b316c41447113b738 and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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