PENTAX Medical Video PROCESSOR EPK-i5500c
by PENTAX Medical Corporation 2 variants
Ref 04961333232895Model EPK-i5500c
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-04961333232895 04961333232895 | Date25 Jun 2026 | StatusActive |
| United States | FDA 510(k) 510(k) | NumberK190805 | Date20 Dec 2019 | 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- Withdrawn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
- EPK-i5500c, 04961333232895
- Primary DI / UDI-DI
- 04961333232895
- Basic UDI-DI
- B-04961333232895
- EMDN Code
- Z12021006 Video nasopharyngo/laryngoscopes
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- JP-MF-000005227
- Authorised representative
- PENTAX Europe GmbH DE-AR-000000006
Other devices from PENTAX Medical Corporation
Properties
Other properties (11)
- Sterile: No
- Implantable: No
- Reusable: No
- Contains Latex: No
- Reprocessed: No
- Human-derived: No
- Human Tissues: No
- Animal Tissues: No
- Administering Medicine: No
- Measuring Function: No
- Incorporates Medicinal Product: No