← Back to catalogue

Widex

FDA UDI

Class II (US FDA UDI)

by Widex A/S

Identity

Trade Name
Widex FDA UDI
Generic Name
Air-conduction hearing aid, canal FDA UDI
Device Name
Widex UNIQUE U-CIC TR (Clay brown ) 440, Left, RC coil, Transverse receiver FDA UDI
Model / Reference
U-CIC FDA UDI
Description
Widex UNIQUE U-CIC TR (Clay brown ) 440, Left, RC coil, Transverse receiver FDA UDI

Identifiers

Catalog Number
8 316 0440 028 FDA UDI
Primary DI / UDI-DI
05706069560404 FDA UDI
FDA Product Code
OSM FDA UDI
GMDN Term
Air-conduction hearing aid, canal 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

Category: Air-conduction hearing aid, canal

Widex by Widex A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Air-conduction hearing aid, canal.

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
Widex A/S

Sources (1)

  • FDA UDI 069dc5c8-324a-4880-8954-bdbb5f388b5a 35 fields · synced May 30, 2026