Taiwan FDA registration 4254c1452547c49f2bc23fcc8dee5191
"Siemens Atellica" α1-Acid Glycoprotein (AAG) (Non-sterile)
TW: "西門子" α1-酸性醣化蛋白質試劑組 (未滅菌)
Taiwan·Risk Class 1·MD·RANDOX LABORATORIES LIMITED·Registered Nov 30, 2017 – Nov 30, 2027ActiveRegistration details
- Analysis ID
- 4254c1452547c49f2bc23fcc8dee5191
- License Form
- Ministry of Health Medical Device Import No. 018560
- Customs Code
- DHA09401856005
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 medical device management method α-1-glycoprotein immunoassay system (C.5420).
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C5420 α-1-glycoprotein immunoassay system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Nov 30, 2017
- Expiry Date
- Nov 30, 2027
About this record
Access comprehensive regulatory information for "Siemens Atellica" α1-Acid Glycoprotein (AAG) (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 4254c1452547c49f2bc23fcc8dee5191 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