Taiwan FDA registration 2cc15d429e7449976f8f2577b4dad67c
"Chongren" oropharyngeal airway tube equipment (unsterilized)
TW: “崇仁”口咽氣道管器材（未滅菌）
Taiwan·Risk Class 1·GALEMED XIAMEN CO., LTD.·Registered Mar 06, 2007 – Mar 06, 2022CancelledRegistration details
- Analysis ID
- 2cc15d429e7449976f8f2577b4dad67c
- Customs Code
- DHA04600034708
Company information
- Manufacturer
- GALEMED XIAMEN CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- GALEMED CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of the oropharyngeal airway tube (D.5110) for the management of medical devices.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5110 Oropharyngeal airway tubes
- Import Information
- Input;; Chinese goods
Dates and status
- Registration Date
- Mar 06, 2007
- Expiry Date
- Mar 06, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Chongren" oropharyngeal airway tube equipment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2cc15d429e7449976f8f2577b4dad67c and manufactured by GALEMED XIAMEN CO., LTD.. The authorized representative in Taiwan is GALEMED CORPORATION.
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