Taiwan FDA registration ee259facda738a5a3ae570ad27cf6bac
"QCMD" EQA Programme (Non-Sterile)
TW: "奎希恩狄" 外部品管計畫 (未滅菌)
Taiwan·Risk Class 1·MD·Quality Control for Molecular Diagnostics (QCMD)·Registered Feb 23, 2023 – Feb 23, 2028ActiveRegistration details
- Analysis ID
- ee259facda738a5a3ae570ad27cf6bac
- License Form
- Ministry of Health Medical Device Import No. 023054
- Customs Code
- DHA09402305400
Company information
- Manufacturer
- Quality Control for Molecular Diagnostics (QCMD)
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EUGENE-CHEN CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment, quality control materials (analytical and non-analytical) (A.1660) the first level identification range.
- 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
- Feb 23, 2023
- Expiry Date
- Feb 23, 2028
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 ee259facda738a5a3ae570ad27cf6bac and manufactured by Quality Control for Molecular Diagnostics (QCMD). The authorized representative in Taiwan is EUGENE-CHEN CO., LTD..
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