Taiwan FDA registration 13a69c3ac2b262ae960b443d5f119fb3
Covidiens nasopharyngeal airway tube (sterilized)
TW: 〝柯惠〞萬靈科鼻咽氣道管(滅菌)
Taiwan·Risk Class 1·COVIDIEN LLC;; COVID·Registered Jun 24, 2011 – Jun 24, 2016CancelledRegistration details
- Analysis ID
- 13a69c3ac2b262ae960b443d5f119fb3
- Customs Code
- DHA04401051009
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Limited to the first level recognition range of the Measures for the Administration of Medical Devices "Nasopharyngeal Airway Tube (D.5100)".
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5100 Nasopharyngeal airway tubes
- Import Information
- Contract manufacturing;; input
Dates and status
- Registration Date
- Jun 24, 2011
- Expiry Date
- Jun 24, 2016
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for Covidiens nasopharyngeal airway tube (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 13a69c3ac2b262ae960b443d5f119fb3 and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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