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More Product Details

Catalog Number

-

Brand Name

Impulse sensors, size 2

Version/Model Number

9800084720010

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)

-

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

KNO

Product Code Name

Accessories, Wheelchair

Device Record Status

Public Device Record Key

3c400299-3340-4bb7-8a89-fca1b50f8518

Public Version Date

July 21, 2022

Public Version Number

1

DI Record Publish Date

July 13, 2022

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"THOMAS HILFEN FÜR KÖRPERBEHINDERTE GMBH & CO. MEDICO KOMMANDITGESELLSCHAFT" Characteristics
Device Class Device Class Description No of Devices
1 A medical device with low to moderate risk that requires general controls 248