Identity
- Trade Name
- Activus FDA UDI
- Generic Name
- Air-conduction hearing aid, behind-the-ear FDA UDI
- Device Name
- Activus HA ACTIVUS LPL N 312-S DGT Hearing Aid FDA UDI
- Model / Reference
- HA ACTIVUS LPL N 312-S DGT FDA UDI
- Description
- Activus HA ACTIVUS LPL N 312-S DGT Hearing Aid FDA UDI
Identifiers
- Catalog Number
- 10955817 FDA UDI
- Primary DI / UDI-DI
- 04056839080924 FDA UDI
- FDA Product Code
- OSM FDA UDI
- GMDN Term
- Air-conduction hearing aid, behind-the-ear FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 874.3305 FDA UDI
- Commercial Distribution
- 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
Yes
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
No
FDA UDI
Category: Air-conduction hearing aid, behind-the-ear
A comprehensive medical device directory listing the Activus HA ACTIVUS LPL N 312-S DGT hearing aid, including its intended use, features, and regulatory compliance.
Similar devices
Also classified as Air-conduction hearing aid, behind-the-ear.
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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
- WS Audiology USA, Inc.
Sources (1)
- FDA UDI 0b03c487-e594-424b-af0c-b06dfd514364 35 fields · synced Aug 3, 2026