Taiwan FDA registration 69cb75bf360937076b77a21ae6c5aff5
“TECHNOPATH” Multi-CHECK Cardiac Control
TW: “泰諾佩斯” 心臟標記品管液
Taiwan·Risk Class 2·MD·TECHNO-PATH MANUFACTURING LTD·Registered Jan 28, 2019 – Jan 28, 2024ExpiredRegistration details
- Analysis ID
- 69cb75bf360937076b77a21ae6c5aff5
- License Form
- Ministry of Health Medical Device Import No. 032159
- Customs Code
- DHA05603215905
Company information
- Manufacturer
- TECHNO-PATH MANUFACTURING LTD
- Manufacturer Country
- Ireland
- Authorized Representative
- EMERGO TAIWAN LIMITED
Product details
- Intended Use
- This product is used for in vitro diagnostic purposes. Use with the AQT90 FLEX analyzer as a liquid serum quality control solution (LQC) for cardiac marker testing.
- 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
- Jan 28, 2019
- Expiry Date
- Jan 28, 2024
About this record
Access comprehensive regulatory information for “TECHNOPATH” Multi-CHECK Cardiac Control in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69cb75bf360937076b77a21ae6c5aff5 and manufactured by TECHNO-PATH MANUFACTURING LTD. The authorized representative in Taiwan is EMERGO TAIWAN LIMITED.
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