Automated External Defibrillator
by ViVest Medical Technology Co., Ltd. 10 variants
Ref VBA03053Model A1 & A3
Active
CE MDR
Valid until
21 Nov 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | Number697310724PB01ET 06973107240805 | Date30 Apr 2026 | StatusActive |
Certificates
- G70 107512 0004 Active
Technical documentation EU MDR
- Certifier
- TÜV SÜD Product Service GmbH 0123
- Issued
- 26 Mar 2026
- Expires
- 21 Nov 2029
- Valid from
- 10 Apr 2026
- Reason
- Change approved
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR Active
Specification
- Device Name
- Automated External Defibrillator
- Model / Reference
- A1 & A3, VBA03053
- Primary DI / UDI-DI
- 06973107240805
- Basic UDI-DI
- 697310724PB01ET
- Direct Marketing DI
- 06973107240805
- EMDN Code
- Z12030501 Semi-automatic defibrillators
- Device Class
- Class III
- EU market of registration
- France
Manufacturer details
- EUDAMED SRN
- CN-MF-000015304
- Authorised representative
- Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001
Other devices from ViVest Medical Technology Co., Ltd.
Properties
Other properties (13)
- 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
- Measuring Function: No
- Incorporates Medicinal Product: No