Taiwan FDA registration 2ffab855f7d528a95bbf4565994c2605

IMMULITE Ferritin Control

TW: 免疫特鐵蛋白品管液
Taiwan flagTaiwan·Risk Class 2·MD·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED·Registered Mar 14, 2018 – Mar 14, 2028Active
Registration details
Analysis ID
2ffab855f7d528a95bbf4565994c2605
License Form
Ministry of Health Medical Device Import No. 030525
Customs Code
DHA05603052507
Company information
Manufacturer Country
United Kingdom
Authorized Representative
SIEMENS HEALTHCARE LIMITED
Product details
Intended Use
This product is an analytical double-concentration tube solution used in IMMULITE/IMMULITE 1000 and IMMULITE 2000 ferritin test sets to assist in monitoring the analytical efficacy of the reagents.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1660 Quality Control Materials (Analytical and Non-Analytical)
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 14, 2018
Expiry Date
Mar 14, 2028
About this record

Access comprehensive regulatory information for IMMULITE Ferritin Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2ffab855f7d528a95bbf4565994c2605 and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS 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