Taiwan FDA registration c719f7196c38664dba47168c00775ed2
Max cerebrospinal fluid detection liquid quality control group
TW: 麥斯腦脊髓液檢測液狀品管組
Registration details
- Analysis ID
- c719f7196c38664dba47168c00775ed2
- Customs Code
- DHA05603419608
Company information
- Manufacturer
- MICROGENICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- This product is used in clinical laboratories as a consistency test sample at known concentrations and can be used to monitor assay conditions in many CSF assays.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Quality control materials (analytical and non-analytical)
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- Jan 18, 2021
- Expiry Date
- Jan 18, 2026
About this record
Access comprehensive regulatory information for Max cerebrospinal fluid detection liquid quality control group in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c719f7196c38664dba47168c00775ed2 and manufactured by MICROGENICS CORPORATION. The authorized representative in Taiwan is THERMO FISHER SCIENTIFIC TAIWAN CO., LTD..
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