Taiwan FDA registration 493038995f526b19e7fd42d99cb322f1
"Dayan" vacuum powered body fluid absorption device (unsterilized)
TW: “大研” 真空動力式體液吸收器具 (未滅菌)
Taiwan·Risk Class 1·DAIKEN MEDICAL CO., LTD.·Registered May 23, 2013 – May 23, 2023ExpiredRegistration details
- Analysis ID
- 493038995f526b19e7fd42d99cb322f1
- Customs Code
- DHA04401304500
Company information
- Manufacturer
- DAIKEN MEDICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN MIN ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Vacuum-powered Body Fluid Absorption Devices (J.6740)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.6740 Vacuum-powered fluid absorption apparatus
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- May 23, 2013
- Expiry Date
- May 23, 2023
About this record
Access comprehensive regulatory information for "Dayan" vacuum powered body fluid absorption device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 493038995f526b19e7fd42d99cb322f1 and manufactured by DAIKEN MEDICAL CO., LTD.. The authorized representative in Taiwan is YUAN MIN ENTERPRISE CO., LTD..
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