MDF® 808 Calibra® Pocket Aneroid Sphygmomanometer + Stethoscope
by MDF Instruments Medifriend Inc. 2 variants
Ref MDF80811Model MDF808
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 | Number69402116808QX 06940211627785 | Date30 Aug 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- Withdrawn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
- Device Name
- MDF® 808 Calibra® Pocket Aneroid Sphygmomanometer + Stethoscope
- Model / Reference
- MDF808, MDF80811
- Primary DI / UDI-DI
- 06940211627785
- Basic UDI-DI
- 69402116808QX
- EMDN Code
- C9006 Aneroid sphygmomanometers
- Device Class
- Class I
- EU market of registration
- Germany
Manufacturer details
- EUDAMED SRN
- CN-MF-000007749
- Authorised representative
- Medical Technology Promedt Consulting GmbH DE-AR-000000085
Other devices from MDF Instruments Medifriend Inc.
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