← Back to catalogue

Unitron

FDA UDI

Class II (US FDA UDI)

by Unitron Hearing

Identity

Trade Name
Unitron FDA UDI
Generic Name
Hearing aid enhanced audio device, telecommunication/multimedia FDA UDI
Device Name
uStream / uTV 3 Bundle FDA UDI
Model / Reference
076-5039-T820 FDA UDI
Description
uStream / uTV 3 Bundle FDA UDI

Identifiers

Catalog Number
076-5039-T820 FDA UDI
Primary DI / UDI-DI
00698764601023 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Hearing aid enhanced audio device, telecommunication/multimedia 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

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
MRI Safety
MR Unsafe FDA UDI

Category: Hearing aid enhanced audio device, telecommunication/multimedia

Unitron by Unitron Hearing — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Hearing aid enhanced audio device, telecommunication/multimedia.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Unitron Hearing

Sources (1)

  • FDA UDI c55c7e50-f434-4781-9c52-6797ecb7b007 35 fields · synced Jun 1, 2026