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Widex

FDA UDI

Class II (US FDA UDI)

by Widex A/S

Identity

Trade Name
Widex FDA UDI
Generic Name
Air-conduction hearing aid, behind-the-ear FDA UDI
Device Name
Widex SUPER220 S2-VSD BTE, Telecoil, Volume control, RC coil FDA UDI
Model / Reference
S2-VSD FDA UDI
Description
Widex SUPER220 S2-VSD BTE, Telecoil, Volume control, RC coil FDA UDI

Identifiers

Catalog Number
8 354 0300 068 FDA UDI
Primary DI / UDI-DI
05706069482942 FDA UDI
510(k) Number
K110973 FDA UDI
FDA Product Code
KLW FDA UDI
GMDN Term
Air-conduction hearing aid, behind-the-ear FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3400 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

No

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 Conditional FDA UDI

Category: Air-conduction hearing aid, behind-the-ear

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, behind-the-ear.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Widex A/S

Sources (1)

  • FDA UDI a953bedc-eb8a-4b54-b79c-68b1e18b2031 36 fields · synced May 30, 2026