Taiwan FDA registration 9460a968a4783fdadc0aa75313ce9204
“Airon” pNeuton Ventilator System
TW: “愛龍”悠騰呼吸器系統
Taiwan·Risk Class 2·MD·Airon Corporation·Registered Apr 08, 2016 – Apr 08, 2026ExpiredRegistration details
- Analysis ID
- 9460a968a4783fdadc0aa75313ce9204
- License Form
- Ministry of Health Medical Device Import No. 028504
- Customs Code
- DHA05602850407
Company information
- Manufacturer
- Airon Corporation
- Manufacturer Country
- United States
- Authorized Representative
- TRANSCORE TAIWAN 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)
- D5895 Continuous breathing apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 08, 2016
- Expiry Date
- Apr 08, 2026
About this record
Access comprehensive regulatory information for “Airon” pNeuton 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 9460a968a4783fdadc0aa75313ce9204 and manufactured by Airon Corporation. The authorized representative in Taiwan is TRANSCORE TAIWAN CO., LTD..
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