Catalog Number

-

Brand Name

Medical Action / Manus

Version/Model Number

AVID274

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"

Yes

For Single-Use

Yes

Prescription Use (Rx)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FRL

Product Code Name

FIBER, MEDICAL, ABSORBENT

Public Device Record Key

3001d4c0-8b3d-48f1-93b2-0a881d26ffea

Public Version Date

June 07, 2019

Public Version Number

4

DI Record Publish Date

December 09, 2016

Package DI Number

30809160116313

Quantity per Package

24

Contains DI Package

20809160116316

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-