Taiwan FDA registration 6a5117d30db2ee3204645d0fc2d649a2
"Proet" laryngeal airway tube (unsterilized)
TW: “普羅艾特”喉頭氣道管 (未滅菌)
Taiwan·Risk Class 1·PROACT MEDICAL LTD.·Registered Dec 24, 2010 – Dec 24, 2015CancelledRegistration details
- Analysis ID
- 6a5117d30db2ee3204645d0fc2d649a2
- Customs Code
- DHA04400974500
Company information
- Manufacturer
- PROACT MEDICAL LTD.
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EVERMEDICAL COMPANY LTD.
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
- import
Dates and status
- Registration Date
- Dec 24, 2010
- Expiry Date
- Dec 24, 2015
- Cancellation Date
- Jun 25, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Proet" laryngeal airway tube (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a5117d30db2ee3204645d0fc2d649a2 and manufactured by PROACT MEDICAL LTD.. The authorized representative in Taiwan is EVERMEDICAL COMPANY LTD..
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