Taiwan FDA registration 05fa5f8e3444a97965c348bc051e0697

“DIAsource”1,25(OH)2-VIT.D-RIA-CT

TW: “百首”1,25維生素D放射免疫分析試劑
Taiwan flagTaiwan·Risk Class 2·MD·DIASOURCE IMMUNOASSAYS S.A.·Registered Feb 27, 2018 – Feb 27, 2023Expired
Registration details
Analysis ID
05fa5f8e3444a97965c348bc051e0697
License Form
Ministry of Health Medical Device Import No. 030511
Customs Code
DHA05603051109
Company information
Manufacturer Country
Belgium
Authorized Representative
TAIWAN LIFE SUPPORT SYSTEMS INC.
Product details
Intended Use
Radioimmunoassay was used to quantitatively detect the content of 1,25-vitamin D in human serum and plasma in vitro.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1825 Vitamin D Test System
Import Information
Imported from abroad
Dates and status
Registration Date
Feb 27, 2018
Expiry Date
Feb 27, 2023
About this record

Access comprehensive regulatory information for “DIAsource”1,25(OH)2-VIT.D-RIA-CT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 05fa5f8e3444a97965c348bc051e0697 and manufactured by DIASOURCE IMMUNOASSAYS S.A.. The authorized representative in Taiwan is TAIWAN LIFE SUPPORT SYSTEMS INC..

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