Avant Pulse Oximeter System
by Nonin Medical, Inc. 5 variants
Ref 9600-1403Model MODEL 9600, 8000SM, PCS-EU
Active
CE MDD 510(k)
Valid until
Not listed
FDA recalls
None foundTrust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-00849686097788 00849686097788 | Date12 Dec 2024 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK023044 | Date23 Jul 2003 | StatusActive |
Certificates
EUDAMED lists no certificate for this device's Basic UDI-DI.
Recalls
No FDA recalls found in the data synced 25 Oct 2026.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- United States
- European Union
Specification
- Model / Reference
- MODEL 9600, 8000SM, PCS-EU, 9600-1403
- Primary DI / UDI-DI
- 00849686097788
- Basic UDI-DI
- B-00849686097788
- EMDN Code
- Z1203020408 Pulse oximeters
- Device Class
- Class IIb
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000008228
- Authorised representative
- MPS Medical Product Service GmbH DE-AR-000005009
Other devices from Nonin Medical, Inc.
Properties
Other properties (10)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Incorporates Medicinal Product: No