Taiwan FDA registration 734494ba6c1db833de5861a6deab5554

"Siemens" lipoprotein A-1 & B correction solution

TW: “西門子” 脂蛋白元A-1 & B校正液
Taiwan flagTaiwan·Risk Class 2·RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.·Registered Nov 27, 2018 – Nov 27, 2028Active
Registration details
Analysis ID
734494ba6c1db833de5861a6deab5554
Customs Code
DHA05603180801
Company information
Manufacturer Country
United Kingdom;;United States
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
This product is intended for in vitro diagnostic use and can be used to correct APOA1 and APO B tests using Atellica CH Analyzer.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1150 Calibrated Products
Import Information
import
Dates and status
Registration Date
Nov 27, 2018
Expiry Date
Nov 27, 2028
About this record

Access comprehensive regulatory information for "Siemens" lipoprotein A-1 & B correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 734494ba6c1db833de5861a6deab5554 and manufactured by RANDOX LABORATORIES LTD.;; Siemens Healthcare Diagnostics Inc.. 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