Taiwan FDA registration a4a49221572e2986f351d2a790032e0c
"Ruimai" dysentery amoeba detection reagent (non-sterilized)
TW: "銳邁" 痢疾阿米巴檢測試劑(未滅菌)
Taiwan·Risk Class 1·OXOID LIMITED;; Remel Europe Limited·Registered Sep 06, 2024 – Sep 06, 2029ActiveRegistration details
- Analysis ID
- a4a49221572e2986f351d2a790032e0c
- Customs Code
- DHA09402359801
Company information
- Manufacturer
- OXOID LIMITED;; Remel Europe Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CREATIVE LIFE SCIENCE CO., LTD.
Product details
- Intended Use
- Limited to the first level of identification of dysentery amoeba serum reagent (C.3220) in the Administrative Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3220 痢疾阿米巴血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Sep 06, 2024
- Expiry Date
- Sep 06, 2029
About this record
Access comprehensive regulatory information for "Ruimai" dysentery amoeba detection reagent (non-sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a4a49221572e2986f351d2a790032e0c and manufactured by OXOID LIMITED;; Remel Europe Limited. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..
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