Taiwan FDA registration 81797c92b4d1429aee4e05963e545571
IMMULITE Cytokine Control Module
TW: 免疫特細胞激素品管試劑
Registration details
- Analysis ID
- 81797c92b4d1429aee4e05963e545571
- License Form
- Ministry of Health Medical Device Import No. 025284
- Customs Code
- DHA05602528404
Company information
- Manufacturer
- SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- SIEMENS HEALTHCARE LIMITED
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- 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
- Sep 11, 2013
- Expiry Date
- Sep 11, 2028
About this record
Access comprehensive regulatory information for IMMULITE Cytokine Control Module in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 81797c92b4d1429aee4e05963e545571 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