Erka. Erkameter 125 Pro
by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft 6 variants
Ref 411.28493.4290, 411.91773.4290, 410.46993.4290, 410.44993.4290, 411.24493.4290, 411.91073.4290, 410.40993.4290, 411.27493.4290, 411.20493.4290, 411.26493.4290Model Erkameter 125 Pro, Erkameter 125
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 | Number42502961411LA | Date25 Sep 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- Withdrawn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
- Trade Name
- Erka. Erkameter 125 ProErka. Erkameter 125
- Device Name
- Erkameter 125 ProErkameter 125
- Model / Reference
- Erkameter 125 Pro, 411.28493.4290, 411.91773.4290, Erkameter 125, 410.46993.4290, 410.44993.4290, 411.24493.4290, 411.91073.4290, 410.40993.4290, 411.27493.4290, 411.20493.4290, 411.26493.4290
- Primary DI / UDI-DI
- 04250296166652, 04250296166720, 04250296166621, 04250296166645, 04250296166690, 04250296166744, 04250296166638, 04250296166669, 04250296166089, 04250296166676
- Basic UDI-DI
- 42502961411LA, 42502961410L8
- EMDN Code
- Z1203020302 Non–invasive blood pressure monitoring instruments
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- DE-MF-000009663
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Properties
Other properties (12)
- 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
- Incorporates Medicinal Product: No