Taiwan FDA registration 8206a557e315a845c7419f76c4e8c8dc
"Siemens" basic phosphate per (diethanolamine method) reagent set
TW: “西門子”鹼性磷酸每 (二乙醇胺法) 試劑組
Taiwan·Risk Class 2·SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.·Registered Apr 09, 2009 – Apr 09, 2024ExpiredRegistration details
- Analysis ID
- 8206a557e315a845c7419f76c4e8c8dc
- Customs Code
- DHA00601998401
Company information
- Manufacturer Country
- United Kingdom;;United States
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- The activity of alkaline phosphate in human serum and plasma is quantitatively determined on the ADVIA automated chemical analysis system.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1050 Alkaline phosphatase or isoenzyme testing system
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Apr 09, 2009
- Expiry Date
- Apr 09, 2024
About this record
Access comprehensive regulatory information for "Siemens" basic phosphate per (diethanolamine method) reagent set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8206a557e315a845c7419f76c4e8c8dc and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS INC.;; RANDOX LABORATORIES LTD.. 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