Taiwan FDA registration 7da0145eb9ad799268eea8493544e7af
"Aris" respirators
TW: "愛瑞司"呼吸器
Taiwan·Risk Class 2·AIROX·Registered Dec 14, 2006 – Dec 14, 2011CancelledRegistration details
- Analysis ID
- 7da0145eb9ad799268eea8493544e7af
- Customs Code
- DHA00601749400
Company information
- Manufacturer
- AIROX
- Manufacturer Country
- France
- Authorized Representative
- BROJAW INC.
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
- Dec 14, 2006
- Expiry Date
- Dec 14, 2011
- Cancellation Date
- Nov 01, 2012
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Aris" respirators in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7da0145eb9ad799268eea8493544e7af and manufactured by AIROX. The authorized representative in Taiwan is BROJAW INC..
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