Taiwan FDA registration 42edadfa6e520b00d814911c065dc226
"Ojie" measles virus IgG antibody reagent (unsterilized)
TW: "歐捷" 麻疹病毒IgG抗體試劑 (未滅菌)
Taiwan·Risk Class 1·ORGENTEC DIAGNOSTIKA GMBH·Registered Apr 13, 2015 – Apr 13, 2025ExpiredRegistration details
- Analysis ID
- 42edadfa6e520b00d814911c065dc226
- Customs Code
- DHA09401510100
Company information
- Manufacturer
- ORGENTEC DIAGNOSTIKA GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- IN FUNG CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of the "Measles Virus Serum Reagent (C.3520)" of the Measures for the Classification and Grading of Medical Devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3520 麻疹病毒血清試劑
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Apr 13, 2015
- Expiry Date
- Apr 13, 2025
About this record
Access comprehensive regulatory information for "Ojie" measles virus IgG antibody reagent (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 42edadfa6e520b00d814911c065dc226 and manufactured by ORGENTEC DIAGNOSTIKA GMBH. The authorized representative in Taiwan is IN FUNG CO., LTD..
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