Taiwan FDA registration 8e3d71c6ed84ff99da2aa1ad76a9ad36
"Dayan" bronchial atresia catheter
TW: “大研”支氣管閉鎖導管
Taiwan·Risk Class 2·DAIKEN MEDICAL CO., LTD.·Registered Oct 09, 2012 – Dec 12, 2027ActiveRegistration details
- Analysis ID
- 8e3d71c6ed84ff99da2aa1ad76a9ad36
- Customs Code
- DHA00601849507
Company information
- Manufacturer
- DAIKEN MEDICAL CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- YUAN MIN ENTERPRISE CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5740 Gas pipe/bronchi divergence gas line
- Import Information
- import
Dates and status
- Registration Date
- Oct 09, 2012
- Expiry Date
- Dec 12, 2027
About this record
Access comprehensive regulatory information for "Dayan" bronchial atresia catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8e3d71c6ed84ff99da2aa1ad76a9ad36 and manufactured by DAIKEN MEDICAL CO., LTD.. The authorized representative in Taiwan is YUAN MIN ENTERPRISE CO., LTD..
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