← Back to catalogue
Ha Contrast Hp+ Demo Bg
EUDAMEDClass IIa (EU MDR)
Ref 10969838Model BTE
by Signia GmbH
Identity
- Trade Name
- HA CONTRAST HP+ DEMO BG EUDAMED
- Model / Reference
- BTE EUDAMED10969838 EUDAMED
Identifiers
- Primary DI / UDI-DI
- 04056839110980 EUDAMED
- Basic UDI-DI
- B-04056839110980 EUDAMED
- EMDN Code
- Y2145060101 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE) EUDAMED
Classification
- Device Class
- Class IIa EUDAMED
- Market of Registration
- Germany EUDAMED
Clinical & Handling
Sterile
No
EUDAMED
Implantable
No
EUDAMED
Reusable
No
EUDAMED
Contains Latex
No
EUDAMED
Reprocessed
No
EUDAMED
CMR Substance
No
EUDAMED
Human-derived
No
EUDAMED
Human Tissues
No
EUDAMED
Animal Tissues
No
EUDAMED
Endocrine Disruptor
No
EUDAMED
Administering Medicine
No
EUDAMED
Measuring Function
No
EUDAMED
Incorporates Medicinal Product
No
EUDAMED
Ha Contrast Hp+ Demo Bg by Signia GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS
Authorization Coverage (European Union — 27 member states)
Regulatory Authorizations
European Union Active
CE/MDD
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04056839110980 | Class IIa | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Signia GmbH
- EUDAMED SRN
- DE-MF-000017173
Sources (1)
- EUDAMED 0c566ed5-daa3-4bc9-8637-d26273524b19 61 fields · synced Jul 30, 2026