Taiwan FDA registration d01867cb5ec1b181887dd8a655a4dfc8
"Covidien" Shirley reinforced endotracheal tube
TW: “柯惠”雪莉加強型氣管內管
Taiwan·Risk Class 2·COVIDIEN LLC;; MALLINCKRODT MEDICAL·Registered Aug 31, 2005 – Aug 31, 2025ExpiredRegistration details
- Analysis ID
- d01867cb5ec1b181887dd8a655a4dfc8
- Customs Code
- DHA00601180105
Company information
- Manufacturer
- COVIDIEN LLC;; MALLINCKRODT MEDICAL
- Manufacturer Country
- Ireland;;United States
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D.5730 Endotracheal tubes
- Import Information
- import
Dates and status
- Registration Date
- Aug 31, 2005
- Expiry Date
- Aug 31, 2025
About this record
Access comprehensive regulatory information for "Covidien" Shirley reinforced endotracheal tube in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d01867cb5ec1b181887dd8a655a4dfc8 and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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