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Auditdata A/S

FDA UDI

Class II (US FDA UDI)

by WS Audiology USA, Inc.

Identity

Trade Name
Auditdata A/S FDA UDI
Generic Name
Audiometric/hearing aid tester FDA UDI
Device Name
UNITY 4 AUD US PACKAGE FDA UDI
Model / Reference
UNITY 4 FDA UDI
Description
UNITY 4 AUD US PACKAGE FDA UDI

Identifiers

Catalog Number
21031174 FDA UDI
Primary DI / UDI-DI
05711781003122 FDA UDI
FDA Product Code
EWO FDA UDI
GMDN Term
Audiometric/hearing aid tester FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.1050 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: Audiometric/hearing aid tester

Auditdata A/S by WS Audiology USA, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Audiometric/hearing aid tester.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 05668a1e-844d-482c-8876-be10c0e762e0 34 fields · synced May 30, 2026