Taiwan FDA registration 2ffab855f7d528a95bbf4565994c2605
IMMULITE Ferritin Control
TW: 免疫特鐵蛋白品管液
Registration details
- Analysis ID
- 2ffab855f7d528a95bbf4565994c2605
- License Form
- Ministry of Health Medical Device Import No. 030525
- Customs Code
- DHA05603052507
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- 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.
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