Taiwan FDA registration c832fcec5034ff271c15368cd4bffe70
“RESMED” Adaptive Servo-Ventilator
TW: “瑞思邁”適應呼吸輔助器
Taiwan·Risk Class 2·MD·RESMED LIMITED·Registered May 24, 2016 – May 24, 2021CancelledRegistration details
- Analysis ID
- c832fcec5034ff271c15368cd4bffe70
- License Form
- Ministry of Health Medical Device Import No. 028540
- Customs Code
- DHA05602854001
Company information
- Manufacturer
- RESMED LIMITED
- Manufacturer Country
- Australia
- Authorized Representative
- BROJAW INC.
Product details
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5895 Continuous breathing apparatus
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- May 24, 2016
- Expiry Date
- May 24, 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” Adaptive Servo-Ventilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c832fcec5034ff271c15368cd4bffe70 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