Taiwan FDA registration cec449ea3848fcba642a62f759c92f1c
"Aon" oropharyngeal airway tube (unsterilized)
TW: "怡安" 口咽氣道管 (未滅菌)
Taiwan·Risk Class 1·HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD·Registered Mar 22, 2011 – Mar 22, 2016CancelledRegistration details
- Analysis ID
- cec449ea3848fcba642a62f759c92f1c
- Customs Code
- DHA04600130602
Company information
- Manufacturer
- HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD
- Manufacturer Country
- China
- Authorized Representative
- LILY MEDICAL 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 22, 2011
- Expiry Date
- Mar 22, 2016
- Cancellation Date
- May 28, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aon" oropharyngeal 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 cec449ea3848fcba642a62f759c92f1c and manufactured by HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.
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