HeartWare HVAD System
by HeartWare, Inc. 10 variants
Ref 1450
Active
CE MDR
Valid until
28 Aug 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberMDR 737528 | Date10 Aug 2026 | StatusActive |
Certificates
- MDR 737528 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 28 Jul 2026
- Expires
- 28 Aug 2029
- Reason
- Change approved
- MDR 737528 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 10 Aug 2026
- Expires
- 28 Aug 2029
- Reason
- Change approved
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- HeartWare HVAD System
- Model / Reference
- 1450
- Primary DI / UDI-DI
- 00763000923570
- Basic UDI-DI
- 0763000B000092489
- EMDN Code
- J01030102 Implantable left monoventricular assistance systems (lvad)
- Device Class
- Class III
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000019976
- Authorised representative
- Medtronic B.V. NL-AR-000006050
Other devices from Heartware Inc.
Properties
Other properties (12)
- Sterile: 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