F&P Airvo
by Fisher & Paykel Healthcare Limited
Ref 900PT562
Active
CE MDR CE MDD
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/MDD | Number94200124KIT01C7 09420012447517 | Date11 Aug 2026 | StatusActive |
| European Union | CE/MDR | Number94200124KIT01C7 09420012447517 | Date11 Aug 2026 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDD, CE/MDR Active
Specification
- Device Name
- Breathing CircuitAirSpiral Tube and Chamber Kit with Nebulizer Adapter
- Model / Reference
- 900PT562
- Primary DI / UDI-DI
- 09420012447517
- Basic UDI-DI
- 94200124KIT01C7, B-09420012447517
- EMDN Code
- R02010199 Standard breathing circuits - other
- Device Class
- Class IIa
- EU market of registration
- Northern Ireland
Manufacturer details
- EUDAMED SRN
- NZ-MF-000002556
- Authorised representative
- FISHER & PAYKEL HEALTHCARE SAS FR-AR-000000294
Other devices from Fisher & Paykel Healthcare, 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