Taiwan FDA registration 267d2582013f1148d6e1cb7156ee6bc8
"Covidien" Nephut bedside patient respiratory monitoring system
TW: “柯惠” 奈普特床邊病患呼吸監測系統
Taiwan·Risk Class 2·COVIDIEN LLC;; Covidien·Registered May 11, 2016 – May 11, 2026ExpiredRegistration details
- Analysis ID
- 267d2582013f1148d6e1cb7156ee6bc8
- Customs Code
- DHA05602853100
Company information
- Manufacturer
- COVIDIEN LLC;; Covidien
- 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)
- E Cardiovascular Medicine Science
- Product Type (Level 2)
- E.2700.
- Import Information
- Input;; Contract manufacturing
Dates and status
- Registration Date
- May 11, 2016
- Expiry Date
- May 11, 2026
About this record
Access comprehensive regulatory information for "Covidien" Nephut bedside patient respiratory monitoring system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 267d2582013f1148d6e1cb7156ee6bc8 and manufactured by COVIDIEN LLC;; Covidien. The authorized representative in Taiwan is MEDTRONIC (TAIWAN) LTD..
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