Taiwan FDA registration 32362be5803b65d53556804d75d3c1e3
"Medegalite" BioSign Flu A+B (Non-Sterile)
TW: "醫德利" 拜篩A+B型流行性感冒快速檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·PRINCETON BIOMEDITECH CORPORATION·Registered May 18, 2018 – May 18, 2023ExpiredRegistration details
- Analysis ID
- 32362be5803b65d53556804d75d3c1e3
- License Form
- Ministry of Health Medical Device Import No. 019066
- Customs Code
- DHA09401906602
Company information
- Manufacturer
- PRINCETON BIOMEDITECH CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- Medley Limited
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Influenza Virus Serum Reagent (C.3330)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3330 Influenza virus serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 18, 2018
- Expiry Date
- May 18, 2023
About this record
Access comprehensive regulatory information for "Medegalite" BioSign Flu A+B (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 32362be5803b65d53556804d75d3c1e3 and manufactured by PRINCETON BIOMEDITECH CORPORATION. The authorized representative in Taiwan is Medley Limited.
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