Taiwan FDA registration 17f0171373498200abba20a9407d87a6
“TUNGSHI” TRINITY RESUSCITATIR SET
TW: “銅璽” 三合一甦醒器組
Taiwan·Risk Class 2·MD·TUNGSHI MEDICAL EQUIPMENT CO., LTD.·Registered Mar 24, 2014 – Mar 24, 2024ExpiredRegistration details
- Analysis ID
- 17f0171373498200abba20a9407d87a6
- License Form
- Ministry of Health Medical Device Manufacturing No. 004550
Company information
- Manufacturer
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- TUNGSHI MEDICAL EQUIPMENT CO., LTD.
Product details
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5925 Powered Emergency Respirator
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 24, 2014
- Expiry Date
- Mar 24, 2024
About this record
Access comprehensive regulatory information for “TUNGSHI” TRINITY RESUSCITATIR SET in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17f0171373498200abba20a9407d87a6 and manufactured by TUNGSHI MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is TUNGSHI MEDICAL EQUIPMENT CO., LTD..
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