Grason-Stadler - Diagnostic Group LLC

Duns Number:175799717

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More Product Details

Catalog Number

-

Brand Name

Grason-Stadler

Version/Model Number

GSI AudioStar Pro

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

May 26, 2020

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code Details

Product Code

EWO

Product Code Name

Audiometer

Device Record Status

Public Device Record Key

71b94ee3-c388-4698-98e6-a3139cc16be0

Public Version Date

May 27, 2020

Public Version Number

3

DI Record Publish Date

November 10, 2016

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"DIAGNOSTIC GROUP LLC" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 32