Taiwan FDA registration 417f9266b76f7113179186955ab084a7
"ResMed" dual positive pressure respiratory assistance system
TW: “瑞思邁”雙陽壓呼吸輔助系統
Taiwan·Risk Class 2·RESMED LIMITED·Registered Jan 10, 2011 – Jan 10, 2021CancelledRegistration details
- Analysis ID
- 417f9266b76f7113179186955ab084a7
- Customs Code
- DHA00602189800
Company information
- Manufacturer
- RESMED LIMITED
- Manufacturer Country
- Australia
- 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
- Jan 10, 2011
- Expiry Date
- Jan 10, 2021
- Cancellation Date
- Aug 09, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "ResMed" dual positive pressure respiratory assistance system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 417f9266b76f7113179186955ab084a7 and manufactured by RESMED LIMITED. 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