Identity
- Trade Name
- GN Hearing FDA UDI
- Generic Name
- Air-conduction hearing aid, receiver-in-canal FDA UDI
- Device Name
- HI,XB762-DRW,HBM,ESP FDA UDI
- Model / Reference
- 22007972 FDA UDI
- Description
- HI,XB762-DRW,HBM,ESP FDA UDI
Identifiers
- Primary DI / UDI-DI
- 05708296223350 FDA UDI
- FDA Product Code
- OSM FDA UDI
- GMDN Term
- Air-conduction hearing aid, receiver-in-canal FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3305 FDA UDI
- Commercial Distribution
- Not in Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
No
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
MR Unsafe FDA UDI
GN Hearing is a high-performance, battery-powered acoustic device designed to compensate for impaired hearing in individuals with mild to profound hearing loss. By transmitting amplified sound waves through an Air-Conduction With Wireless Technology (ACWT) receiver-in-canal (RIC), the device enables computerized adjustments and tailored sound processing for improved listening experiences.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
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Manufacturer
- Manufacturer
- Gn Hearing A/S
Sources (1)
- FDA UDI cc8e04c7-8f0c-406f-b021-64bbadee54c6 35 fields · synced Jul 11, 2026