Defibrillator/Monitor
by Shenzhen Mindray Bio-Medical Electronics Co., Ltd. 10 variants
Ref Defibrillator/MonitorModel BeneHeart D30
Expiring
CE MDR
Valid until
25 Oct 2027
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 757846 | Date20 Aug 2026 | StatusExpiring |
Certificates
- MDR 757846 Expiring
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 20 Aug 2026
- Expires
- 25 Oct 2027
- Reason
- Other
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Expiring
Specification
- Device Name
- Defibrillator/Monitor
- Model / Reference
- BeneHeart D30, Defibrillator/Monitor
- Primary DI / UDI-DI
- 06903053025270
- Basic UDI-DI
- 69449040AB010000102Z
- EMDN Code
- Z12030501, Z12030502
- Device Class
- Class III
- 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