Taiwan FDA registration e896ecd68b9ac67e3b95fca4d5ae60eb
“QCMD” EQA Programme (Non-Sterile)
TW: “康西恩”外部品管計劃(未滅菌)
Taiwan·Risk Class 1·MD·Quality Control for Molecular Diagnostics (QCMD)·Registered Oct 25, 2019 – Oct 25, 2024ExpiredRegistration details
- Analysis ID
- e896ecd68b9ac67e3b95fca4d5ae60eb
- License Form
- Ministry of Health Medical Device Import No. 020982
- Customs Code
- DHA09402098200
Company information
- Manufacturer
- Quality Control for Molecular Diagnostics (QCMD)
- Manufacturer Country
- United Kingdom
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of quality control materials (analytical and non-analytical) (A.1660) of the Measures for the Administration of Medical Devices.
- 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
- Oct 25, 2019
- Expiry Date
- Oct 25, 2024
About this record
Access comprehensive regulatory information for “QCMD” EQA Programme (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e896ecd68b9ac67e3b95fca4d5ae60eb and manufactured by Quality Control for Molecular Diagnostics (QCMD). The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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