Erka. Erkaphon Duo
by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft 4 variants
Ref 541.00010.7590, 541.00020.7590, 541.00051.7590, 541.00080.7590, 541.00060.7590, 541.00055.7590, 541.00025.7590Model Erkaphon Duo
Active
CE MDR
Valid until
Not listed
FDA recalls
Not applicable
Documents
None, self-declared
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number42502961541LQ | Date29 Sep 2025 | StatusActive |
Certificates
No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Erkaphon Duo
- Model / Reference
- Erkaphon Duo, 541.00010.7590, 541.00020.7590, 541.00051.7590, 541.00080.7590, 541.00060.7590, 541.00055.7590, 541.00025.7590
- Primary DI / UDI-DI
- 04250296129169, 04250296129190, 04250296156141, 04250296150613, 04250296129244, 04250296156134, 04250296150590
- Basic UDI-DI
- 42502961541LQ
- EMDN Code
- C9005 Phonendoscopes and stethoscopes
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000009663
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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