Taiwan FDA registration f5016b3f6221254262dd541990ac0dca
Max Integrative Immunoassay Liquid Quality Control Group
TW: 麥斯整合型免疫分析液狀品管組
Registration details
- Analysis ID
- f5016b3f6221254262dd541990ac0dca
- Customs Code
- DHA05603417309
Company information
- Manufacturer
- MICROGENICS CORPORATION
- Manufacturer Country
- United States
- Authorized Representative
- THERMO FISHER SCIENTIFIC TAIWAN CO., LTD.
Product details
- Intended Use
- This product can be used to monitor the verification conditions during clinical laboratory 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
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- Dec 15, 2020
- Expiry Date
- Dec 15, 2025
About this record
Access comprehensive regulatory information for Max Integrative Immunoassay 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 f5016b3f6221254262dd541990ac0dca 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