Taiwan FDA registration b76f7620c558ccc5b1d755bc3380ea0d
"Dybo" Diarrhoeagenic E coli PCR kit (Non-Sterile)
TW: "帝博"大腸桿菌微生物鑑定試劑套組(未滅菌)
Taiwan·Risk Class 1·MD·SSI Diagnostica·Registered Nov 02, 2018 – Nov 02, 2023ExpiredRegistration details
- Analysis ID
- b76f7620c558ccc5b1d755bc3380ea0d
- License Form
- Ministry of Health Medical Device Import No. 019768
- Customs Code
- DHA09401976808
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 "E. coli Serological Reagent (C.3255)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C3255 E. coli serum reagent
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 02, 2018
- Expiry Date
- Nov 02, 2023
About this record
Access comprehensive regulatory information for "Dybo" Diarrhoeagenic E coli PCR kit (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 b76f7620c558ccc5b1d755bc3380ea0d and manufactured by SSI Diagnostica. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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