Defibtech 9V battery
Ref DAC-410-100Model DDU series
Active
CE MDR CE MDD
Valid until
13 Nov 2029
FDA recalls
Not applicable
Documents
Trust
Unverified
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDR | NumberB-00815098020850 00815098020850 | Date13 Oct 2026 | StatusActive |
| European Union | CE/MDD | NumberB-00815098020850 00815098020850 | Date13 Oct 2026 | StatusActive |
Certificates
- MDR 781624 Active
Technical documentation EU MDR
- Certifier
- BSI Group The Netherlands B.V. 2797
- Issued
- 21 Sep 2026
- Expires
- 13 Nov 2029
- Reason
- Add device or group
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
European Union — CE/MDR, CE/MDD Active
Specification
- Device Name
- 9V battery for use with DDU-1XX AED
- Model / Reference
- DAC-410-100, DDU series
- Primary DI / UDI-DI
- 00815098020850
- Basic UDI-DI
- B-00815098020850, 081509802DDUE3
- EMDN Code
- Z12030580 Defibrillators - hardware accessories
- Device Class
- Class IIbClass III
- EU market of registration
- Netherlands
Manufacturer details
- EUDAMED SRN
- US-MF-000012146
- Authorised representative
- Emergo Europe B.V. NL-AR-000000116
Other devices from Defibtech, L.L.C.
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