Taiwan FDA registration 43872411495a521226fac96c3635ab48
"Arox" Prolux respirator
TW: “艾羅克斯”普樂士呼吸器
Taiwan·Risk Class 2·AIROX·Registered Mar 27, 2008 – Mar 27, 2013CancelledRegistration details
- Analysis ID
- 43872411495a521226fac96c3635ab48
- Customs Code
- DHA00601875102
Company information
- Manufacturer
- AIROX
- Manufacturer Country
- France
- 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)
- D Anesthesiology
- Product Type (Level 2)
- D.5895 Continuous respirators
- Import Information
- import
Dates and status
- Registration Date
- Mar 27, 2008
- Expiry Date
- Mar 27, 2013
- Cancellation Date
- Jan 17, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Arox" Prolux respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 43872411495a521226fac96c3635ab48 and manufactured by AIROX. The authorized representative in Taiwan is Taiwan Covidien Corporation Limited.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices