Taiwan FDA registration 67c4260bc7ffe343c42dd48228db36a6
"Aerox" Rayzhenda respirator
TW: “艾羅克斯”雷震達呼吸器
Registration details
- Analysis ID
- 67c4260bc7ffe343c42dd48228db36a6
- Customs Code
- DHA00601875000
Company information
- Manufacturer
- AIROX
- Manufacturer Country
- France
- Authorized Representative
- Taiwan Covidien Corporation Limited
Product details
- Intended Use
- Vacuum.
- 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
- Feb 24, 2014
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aerox" Rayzhenda respirator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 67c4260bc7ffe343c42dd48228db36a6 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.
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