Taiwan FDA registration 3256d6bc5cf59a2ca40bfbc0fae34baf
"Siemens" 120 optical test material
TW: "西門子" 120光學試驗材料
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; FISHER DIAGNOSTICS·Registered May 02, 2006 – May 02, 2026ExpiredRegistration details
- Analysis ID
- 3256d6bc5cf59a2ca40bfbc0fae34baf
- Customs Code
- DHA00601652009
Company information
- Manufacturer Country
- United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Adjust the magnification factor of the ADVIA 120 hematology analyzer.
- Product Type (Level 1)
- B Hematology, pathology, and genetics
- Product Type (Level 2)
- B.8625 Hematology Quality Control Mixtures
- Import Information
- import
Dates and status
- Registration Date
- May 02, 2006
- Expiry Date
- May 02, 2026
About this record
Access comprehensive regulatory information for "Siemens" 120 optical test material in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3256d6bc5cf59a2ca40bfbc0fae34baf 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