Taiwan FDA registration e994b667a57681d8624cf9dd3b0f8f75
"Laili" oropharyngeal airway tube (unsterilized)
TW: “萊禮”口咽氣道管 (未滅菌)
Taiwan·Risk Class 1·HSINER CO., LTD.·Registered Dec 09, 2008 – Dec 09, 2018CancelledRegistration details
- Analysis ID
- e994b667a57681d8624cf9dd3b0f8f75
- Customs Code
- DHY04300231409
Company information
- Manufacturer
- HSINER CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TAIWAN STANCH CO., 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
- Domestic;; Contract manufacturing
Dates and status
- Registration Date
- Dec 09, 2008
- Expiry Date
- Dec 09, 2018
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Laili" 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 e994b667a57681d8624cf9dd3b0f8f75 and manufactured by HSINER CO., LTD.. The authorized representative in Taiwan is TAIWAN STANCH CO., LTD..
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