Erka. Perfekt Klinik
by ERKA Kallmeyer Medizintechnik GmbH & Co. Kommanditgesellschaft 5 variants
Ref 215.28482.7290, 214.24482.7290, 215.27482.7290, 214.26482.7290, 215.29482.7290, 214.27482.7290, 215.26482.7290Model Perfekt Klinik
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 | Number42502961214L6 | Date24 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- Withdrawn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
- Device Name
- Perfekt Klinik
- Model / Reference
- Perfekt Klinik, 215.28482.7290, 214.24482.7290, 215.27482.7290, 214.26482.7290, 215.29482.7290, 214.27482.7290, 215.26482.7290
- Primary DI / UDI-DI
- 04250296152723, 04250296152907, 04250296152754, 04250296152884, 04250296152792, 04250296152877, 04250296152761
- Basic UDI-DI
- 42502961214L6
- EMDN Code
- C9006 Aneroid sphygmomanometers
- Device Class
- Class I
- 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