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Real-Ear

FDA UDI

Class II (US FDA UDI)

by WS Audiology USA, Inc.

Identity

Trade Name
REAL-EAR FDA UDI
Generic Name
Audiometric/hearing aid tester FDA UDI
Device Name
REAL-EAR DC ADAPTOR (AUD/REM) FDA UDI
Model / Reference
REAL-EAR DC ADAPTOR (AUD/REM) FDA UDI
Description
REAL-EAR DC ADAPTOR (AUD/REM) FDA UDI

Identifiers

Catalog Number
10823944 FDA UDI
Primary DI / UDI-DI
05711781000206 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Audiometric/hearing aid tester

Real-Ear 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 67567bfd-b12e-46f8-94db-b4d91fa139fe 35 fields · synced Jun 8, 2026