Taiwan FDA registration 19135103ba7cbcad8fd9519114b2b469
"Dybo" Escherichia coli Antisera Reagent (Non-Sterile)
TW: "帝博" 大腸桿菌抗血清試劑(未滅菌)
Taiwan·Risk Class 1·MD·SSI Diagnostica·Registered Oct 31, 2019 – Oct 31, 2024ExpiredRegistration details
- Analysis ID
- 19135103ba7cbcad8fd9519114b2b469
- License Form
- Ministry of Health Medical Device Import No. 020994
- Customs Code
- DHA09402099404
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
- Oct 31, 2019
- Expiry Date
- Oct 31, 2024
About this record
Access comprehensive regulatory information for "Dybo" Escherichia coli 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 19135103ba7cbcad8fd9519114b2b469 and manufactured by SSI Diagnostica. The authorized representative in Taiwan is DYBO ENTERPRISE COMPANY LIMITED.
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