audifon - RITE Tinnitus - audifon GmbH & Co. KG

Duns Number:344064407

Device Description: RITE Tinnitus

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More Product Details

Catalog Number

025381-9507-3159-1720

Brand Name

audifon

Version/Model Number

sueno pro R

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

K130417

Product Code Details

Product Code

KLW

Product Code Name

Masker, Tinnitus

Device Record Status

Public Device Record Key

1012fee2-1b9c-4821-8f41-d919b9c55af6

Public Version Date

October 06, 2020

Public Version Number

2

DI Record Publish Date

March 08, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"AUDIFON GMBH & CO. KG" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 262
2 A medical device with a moderate to high risk that requires special controls. 166