Taiwan FDA registration f093de1ced513e0cfc96abfb0b563629
Synergium pneumoniae antibody kit (unsterilized)
TW: 協克黴漿菌肺炎抗體試劑套組(未滅菌)
Taiwan·Risk Class 1·SAVYON DIAGNOSTICS LTD.·Registered Mar 01, 2010 – Mar 01, 2030ActiveRegistration details
- Analysis ID
- f093de1ced513e0cfc96abfb0b563629
- Customs Code
- DHA04400857608
Company information
- Manufacturer
- SAVYON DIAGNOSTICS LTD.
- Manufacturer Country
- Israel
- Authorized Representative
- SEEKERS BIOMEDICAL CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.3375 黴漿菌屬血清試劑
- Import Information
- import
Dates and status
- Registration Date
- Mar 01, 2010
- Expiry Date
- Mar 01, 2030
About this record
Access comprehensive regulatory information for Synergium pneumoniae 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 f093de1ced513e0cfc96abfb0b563629 and manufactured by SAVYON DIAGNOSTICS LTD.. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices