Taiwan FDA registration 22f851efa5ec30245eae9e9a3300d44e
"Auswedish Kneput handheld carbon dioxide/oximeter
TW: “奧瑞典” 耐普特手持式二氧化碳/血氧濃度計
Taiwan·Risk Class 2·ORIDION MEDICAL 1987 LTD.;; COVIDIEN LLC·Registered Dec 11, 2015 – Dec 11, 2020CancelledRegistration details
- Analysis ID
- 22f851efa5ec30245eae9e9a3300d44e
- Customs Code
- DHA05602787307
Company information
- Manufacturer
- ORIDION MEDICAL 1987 LTD.;; COVIDIEN LLC
- Manufacturer Country
- Israel;;United States
- Authorized Representative
- Taiwan Covidien Corporation Limited
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
- Dec 11, 2015
- Expiry Date
- Dec 11, 2020
- Cancellation Date
- Mar 16, 2017
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Auswedish Kneput handheld carbon dioxide/oximeter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 22f851efa5ec30245eae9e9a3300d44e and manufactured by ORIDION MEDICAL 1987 LTD.;; COVIDIEN LLC. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
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