Bio-Logic AudX - The AuDX Otoacoustic Emissions Measurement System - NATUS MEDICAL INCORPORATED

Duns Number:962519208

Device Description: The AuDX Otoacoustic Emissions Measurement System Basic box with DPOAE produces controlled The AuDX Otoacoustic Emissions Measurement System Basic box with DPOAE produces controlled acoustic signals in the earcanal and measures the resulting evoked otoacoustic emissions (OAEs) that are generated by the outer hair cells of the inner ear as a result of normal peripheral hearing processes. The AuDX device performs both transient evoked otoacoustic emissions (TEOAE) and distortion product otoacoustic emissions (DPOAE) tests that can be utilized in hearing screening and diagnostic test environments.

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More Product Details

Catalog Number

014381

Brand Name

Bio-Logic AudX

Version/Model Number

014381

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

MRI safety Status

Labeling does not contain MRI Safety Information

Device required to be labeled as containing natural rubber latex or dry natural rubber (21 CFR 801.437)

-

Device labeled as "Not made with natural rubber latex"

-

For Single-Use

-

Prescription Use (Rx)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K111618

Product Code Details

Product Code

EWO

Product Code Name

Audiometer

Device Record Status

Public Device Record Key

5a234bcf-a3df-4691-96e7-3b19151670a5

Public Version Date

January 17, 2019

Public Version Number

1

DI Record Publish Date

December 17, 2018

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"NATUS MEDICAL INCORPORATED" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 24
2 A medical device with a moderate to high risk that requires special controls. 302
3 A medical device with high risk that requires premarket approval 5