Taiwan FDA registration ac1a9ab1cc78809fc9d968e178e73997
"Covidien" Shirley laser through the endotracheal tube
TW: "柯惠"雪莉雷射經口氣管內管
Taiwan·Risk Class 2·COVIDIEN LLC;; MALLINCKRODT MEDICAL·Registered Nov 21, 2005 – Nov 21, 2025ExpiredRegistration details
- Analysis ID
- ac1a9ab1cc78809fc9d968e178e73997
- Customs Code
- DHA00601361202
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
- Nov 21, 2005
- Expiry Date
- Nov 21, 2025
About this record
Access comprehensive regulatory information for "Covidien" Shirley laser through the 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 ac1a9ab1cc78809fc9d968e178e73997 and manufactured by COVIDIEN LLC;; MALLINCKRODT MEDICAL. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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