Taiwan FDA registration f2e1ec79576023d640af2652d3797abf
Xiecke trachoma antibody kit (unsterilized)
TW: 協克砂眼型披衣菌抗體試劑套組(未滅菌)
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Mar 01, 2010 – Mar 01, 2030ActiveRegistration details
- Analysis ID
- f2e1ec79576023d640af2652d3797abf
- Customs Code
- DHA04400857700
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- It is limited to the first-level identification scope of Chlamydia serum reagent (C.3120) in the classification and grading management measures for medical devices.
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3120 披衣菌血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Mar 01, 2010
- Expiry Date
- Mar 01, 2030
About this record
Access comprehensive regulatory information for Xiecke trachoma antibody kit (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f2e1ec79576023d640af2652d3797abf and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
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