Positive Airway Pressure System (PAP System)
by Resvent Medical Technology Co., Ltd. 11 variants
Ref iBreeze 20A ProModel iBreeze 20C, iBreeze 20A
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None linked in EUDAMED
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697081942iBreeze20CZ5 06970819423311 | Date15 Apr 2025 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Positive Airway Pressure System(PAP System)
- Model / Reference
- iBreeze 20C, iBreeze 20A, iBreeze 20A Pro
- Primary DI / UDI-DI
- 06970819423311
- Basic UDI-DI
- 697081942iBreeze20CZ5
- EMDN Code
- Z12030102 Continuous positive pressure equipment
- Device Class
- Class IIa
- EU market of registration
- Spain
Manufacturer details
- EUDAMED SRN
- CN-MF-000012608
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Resvent Medical Technology Co., Ltd.
Properties
Other properties (13)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- CMR Substance: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Endocrine Disruptor: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No