Catalog Number

-

Brand Name

Medical Action / Manus

Version/Model Number

AVID272

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

February 26, 2019

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

61814056-dc54-4c9d-a4aa-fa35afb42cfe

Public Version Date

June 07, 2019

Public Version Number

5

DI Record Publish Date

December 09, 2016

Package DI Number

30809160116351

Quantity per Package

48

Contains DI Package

20809160116354

Package Discontinue Date

February 26, 2019

Package Status

Not in Commercial Distribution

Package Type

-