Taiwan FDA registration 343fbb3ea6639fc0d0c44477dc37614c
"Covidien" nasopharyngeal airway tube (sterilized)
TW: "柯惠" 鼻咽氣道管 (滅菌)
Taiwan·Risk Class 1·COVIDIEN LLC;; COVID·Registered May 21, 2014 – May 21, 2029ActiveRegistration details
- Analysis ID
- 343fbb3ea6639fc0d0c44477dc37614c
- Customs Code
- DHA09401415706
Company information
- Manufacturer
- COVIDIEN LLC;; COVID
- Manufacturer Country
- Mexico;;United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- Limited to the classification and grading management of medical equipment "nasopharyngeal airway tube (D.5100)" level identification range.
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5100 Nasopharyngeal airway tubes
- Import Information
- QMS/QSD;; 輸入
Dates and status
- Registration Date
- May 21, 2014
- Expiry Date
- May 21, 2029
About this record
Access comprehensive regulatory information for "Covidien" 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 343fbb3ea6639fc0d0c44477dc37614c and manufactured by COVIDIEN LLC;; COVID. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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