Taiwan FDA registration e3226c7e9df700e04b4e0c06917894be
"Siemens" CO2 corrector/diluent
TW: “西門子”二氧化碳校正品/稀釋液
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered Nov 27, 2009 – Nov 27, 2029ActiveRegistration details
- Analysis ID
- e3226c7e9df700e04b4e0c06917894be
- Customs Code
- DHA00602073302
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- In vitro diagnostics uses enzyme assays that correct carbon dioxide on different Siemens instruments.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1150 Calibrated Products
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Nov 27, 2009
- Expiry Date
- Nov 27, 2029
About this record
Access comprehensive regulatory information for "Siemens" CO2 corrector/diluent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e3226c7e9df700e04b4e0c06917894be and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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