Taiwan FDA registration 9fdf6cadcdf3c62b9bd4a244203546f2
“Covidien” Puritan Bennett 980 Ventilator System
TW: “柯惠”奈普特呼吸器
Taiwan·Risk Class 2·MD·COVIDIEN·Registered Aug 20, 2015 – Aug 20, 2025CancelledRegistration details
- Analysis ID
- 9fdf6cadcdf3c62b9bd4a244203546f2
- License Form
- Ministry of Health Medical Device Import No. 027603
- Customs Code
- DHA05602760304
Company information
- Manufacturer
- COVIDIEN
- Manufacturer Country
- Ireland
- Authorized Representative
- MEDTRONIC (TAIWAN) LTD.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 20, 2015
- Expiry Date
- Aug 20, 2025
- Cancellation Date
- Sep 21, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for “Covidien” Puritan Bennett 980 Ventilator System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9fdf6cadcdf3c62b9bd4a244203546f2 and manufactured by COVIDIEN. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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