Taiwan FDA registration 668f3437755774beaa7f813759e1411c
“Airsonett” Medical Mobile Air Cleaner
TW: “艾爾索尼”醫療專用空氣清淨儀
Taiwan·Risk Class 2·MD·Airsonett, AB·Registered Apr 20, 2015 – Apr 20, 2020CancelledRegistration details
- Analysis ID
- 668f3437755774beaa7f813759e1411c
- License Form
- Ministry of Health Medical Device Import No. 027162
- Customs Code
- DHA05602716200
Company information
- Manufacturer
- Airsonett, AB
- Manufacturer Country
- Sweden
- Authorized Representative
- REVO LASER CORPORATION
Product details
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J5045 Medical Recirculation Air Purifier
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Apr 20, 2015
- Expiry Date
- Apr 20, 2020
- Cancellation Date
- Jun 22, 2022
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for “Airsonett” Medical Mobile Air Cleaner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 668f3437755774beaa7f813759e1411c and manufactured by Airsonett, AB. The authorized representative in Taiwan is REVO LASER CORPORATION.
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