Catalog Number

5075

Brand Name

A-V Impulse

Version/Model Number

5075

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

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

-

Product Code

JOW

Product Code Name

SLEEVE, LIMB, COMPRESSIBLE

Public Device Record Key

96d48021-64af-4d36-b5e2-32d6ff6da686

Public Version Date

February 15, 2019

Public Version Number

4

DI Record Publish Date

September 24, 2016

Package DI Number

10884521077379

Quantity per Package

4

Contains DI Package

20884521077376

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE