Taiwan FDA registration 41b956b5acf1bd4e932c322b0f9417e4
"Siemens Atellica" Phosphorus (inorganic) reagent (Non-Sterile)
TW: "西門子"無機磷檢測試劑(未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LIMITED·Registered Sep 11, 2017 – Sep 11, 2027ActiveRegistration details
- Analysis ID
- 41b956b5acf1bd4e932c322b0f9417e4
- License Form
- Ministry of Health Medical Device Import No. 018292
- Customs Code
- DHA09401829206
Company information
- Manufacturer
- RANDOX LABORATORIES LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- Limited to the first level identification range of the phosphoric acid (inorganic) test system (A.1580) of the management measures for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1580 Phosphoric acid (inorganic) test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Sep 11, 2017
- Expiry Date
- Sep 11, 2027
About this record
Access comprehensive regulatory information for "Siemens Atellica" Phosphorus (inorganic) reagent (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 41b956b5acf1bd4e932c322b0f9417e4 and manufactured by RANDOX LABORATORIES LIMITED. 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