Ha Motion Sp 3px Gr
EUDAMEDFDA UDIClass IIa (EU MDR)
by Signia GmbH
Identity
- Trade Name
- HA MOTION SP 3PX GR EUDAMEDSignia Siemens FDA UDI
- Generic Name
- Air-conduction hearing aid, behind-the-ear FDA UDI
- Device Name
- Signia Siemens HA MOTION SP 3PX GR Hearing Aid FDA UDI
- Model / Reference
- BTE EUDAMED10942727 EUDAMEDHA MOTION SP 3PX GR FDA UDI
- Description
- Signia Siemens HA MOTION SP 3PX GR Hearing Aid FDA UDI
Identifiers
- Catalog Number
- 10942727 FDA UDI
- Primary DI / UDI-DI
- 04038953855794 EUDAMEDFDA UDI
- Basic UDI-DI
- B-04038953855794 EUDAMED
- FDA Product Code
- OSM FDA UDI
- EMDN Code
- Y2145060101 BEHIND-THE-EAR HEARING AIDS WITH RECEIVER IN THE DEVICE (BTE) EUDAMED
- GMDN Term
- Air-conduction hearing aid, behind-the-ear FDA UDI
Classification
- Device Class
- Class IIa EUDAMEDClass II FDA UDI
- Regulation Number
- 874.3305 FDA UDI
- Market of Registration
- Germany EUDAMED
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
Single Use
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
Prescription Use
Yes
Over-the-Counter
No
Convenience Kit
No
Combination Product
No
HCT/P
No
Premarket Exempt
Yes
Lot / Batch Number
No
Serial Number
Yes
Expiration Date
No
Manufacturing Date
No
Category: Air-conduction hearing aid, behind-the-ear
Ha Motion Sp 3px Gr by Signia GmbH — Class IIa — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Air-conduction hearing aid, behind-the-ear.
- Oticon — Oticon A/S · Class II
- Amplifon — Sonova AG · Class II
- Phonak Naída L30-SP — Sonova AG · Class II
- Phonak — Phonak, Inc. · Class II
- GN ReSound — Gn Hearing A/S · Class II
- Miracle-Ear — WS Audiology USA, Inc. · Class II
- NUEAR — Starkey Laboratories Inc. · Class II
- HHM — Oticon A/S · Class II
Authorization Coverage (2 countries)
Regulatory Authorizations
CE/MDD
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| EUDAMED | European Union | CE/MDD | B-04038953855794 | Class IIa | Active |
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class IIa | Pending data |
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Manufacturer
- Manufacturer
- Signia GmbH
- EUDAMED SRN
- DE-MF-000017173
Sources (2)
- EUDAMED 06d56000-c6c2-43b9-b170-d9845fdd488b 61 fields · synced Jun 19, 2026
- FDA UDI 01a656cc-bfca-40b7-b9b6-19b3ec92e884 36 fields · synced May 30, 2026