Taiwan FDA registration 492faf85846a4a0908a6fc04ecd32196
"Siemens Atellica" Iron reagent (Non-Sterile)
TW: "西門子"鐵檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LIMITED·Registered Sep 11, 2017 – Sep 11, 2027ActiveRegistration details
- Analysis ID
- 492faf85846a4a0908a6fc04ecd32196
- License Form
- Ministry of Health Medical Device Import No. 018295
- Customs Code
- DHA09401829502
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 Measures for the Administration of Medical Devices "Iron (Non-blood Matrix) Test System (A.1410)".
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1410 Iron (non-blood matrix) 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" Iron 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 492faf85846a4a0908a6fc04ecd32196 and manufactured by RANDOX LABORATORIES LIMITED. The authorized representative in Taiwan is SIEMENS HEALTHCARE LIMITED.
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