Taiwan FDA registration f8db63680d3c4c62598304a4913782b3
Nofasiderence amoeba immunoglobulin G enzyme immunoassay kit (unsterilized)
TW: 諾法鐵痢疾阿米巴免疫球蛋白G酵素免疫分析試劑套組(未滅菌)
Taiwan·Risk Class 1·GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH·Registered Mar 10, 2022 – Mar 10, 2027ActiveRegistration details
- Analysis ID
- f8db63680d3c4c62598304a4913782b3
- Customs Code
- DHA09402275509
Company information
- Manufacturer
- GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Classification and Grading Management Measures for Medical Devices Limited to the Identification Range of the First Grade of Dysentery Amoeba Serological Reagent (C.3220).
- 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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Mar 10, 2022
- Expiry Date
- Mar 10, 2027
About this record
Access comprehensive regulatory information for Nofasiderence amoeba immunoglobulin G enzyme immunoassay 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 f8db63680d3c4c62598304a4913782b3 and manufactured by GOLD STANDARD DIAGNOSTICS FRANKFURT GMBH. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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