Taiwan FDA registration c2ed19efb65798ad05c574201a05030f
"Randox" Tri-Level Cardiac Control
TW: "瑞德士" 心臟標記品管液
Registration details
- Analysis ID
- c2ed19efb65798ad05c574201a05030f
- License Form
- Ministry of Health Medical Device Import No. 033469
- Customs Code
- DHA05603346902
Company information
- Manufacturer
- RANDOX LABORATORIES LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- KUO'S YUAN IN ENTERPRISE CO., LTD.
Product details
- Intended Use
- This product is used in vitro diagnosis as a quality control for clinical biochemical and immune system cardiac marker testing items.
- 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
- Apr 09, 2020
- Expiry Date
- Apr 09, 2025
About this record
Access comprehensive regulatory information for "Randox" Tri-Level 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 c2ed19efb65798ad05c574201a05030f and manufactured by RANDOX LABORATORIES LTD.. The authorized representative in Taiwan is KUO'S YUAN IN ENTERPRISE CO., LTD..
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