Catalog Number

-

Brand Name

MEDI

Version/Model Number

AK2M5W2

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 20, 2020

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

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

IPM

Product Code Name

COVER, LIMB

Public Device Record Key

52c26048-636d-4839-abdf-984ecddc7a53

Public Version Date

November 23, 2021

Public Version Number

4

DI Record Publish Date

November 20, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-