Taiwan FDA registration 14cef5f03372b9ada5a586a0e8a1d505
"Dybo" Salmonella Antisera Reagent (Non-Sterile)
TW: "帝博"沙門氏菌抗血清試劑(未滅菌)
Taiwan·Risk Class 1·MD·SSI Diagnostica·Registered Oct 03, 2019 – Oct 03, 2024ExpiredRegistration details
- Analysis ID
- 14cef5f03372b9ada5a586a0e8a1d505
- License Form
- Ministry of Health Medical Device Import No. 020918
- Customs Code
- DHA09402091801
Company information
- Manufacturer
- SSI Diagnostica
- Manufacturer Country
- Denmark
- Authorized Representative
- DYBO ENTERPRISE COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Salmonella Serological Reagent (C.3550)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3550 Salmonella serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Oct 03, 2019
- Expiry Date
- Oct 03, 2024
About this record
Access comprehensive regulatory information for "Dybo" Salmonella Antisera Reagent (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 14cef5f03372b9ada5a586a0e8a1d505 and manufactured by SSI Diagnostica. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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