Electrocardiograph
by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. 10 variants
Ref BeneHeart R3AModel BeneHeart R12/BeneHeart R12B/BeneHeart R12A/BeneHeart R3/BeneHeart R3B/BeneHeart R3A
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 | Number69449040AB010000563R 06944904040233 | Date29 Apr 2026 | 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- Withdrawn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
- Model / Reference
- BeneHeart R12/BeneHeart R12B/BeneHeart R12A/BeneHeart R3/BeneHeart R3B/BeneHeart R3A, BeneHeart R3A
- Primary DI / UDI-DI
- 06944904040233
- Basic UDI-DI
- 69449040AB010000563R
- EMDN Code
- Z12050301 General purpose electrocardiographs
- Device Class
- Class IIa
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000014156
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
See all devices from Shenzhen Mindray Bio-Medical Electronics Co., Ltd. →
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