Catalog Number

Not Applicable

Brand Name

MedSource Extrication Device

Version/Model Number

MS-ED3000

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

CCX

Product Code Name

Support, Patient Position

Public Device Record Key

0ebff32b-96e6-4f1c-97ba-6a8e72c421e2

Public Version Date

June 10, 2022

Public Version Number

2

DI Record Publish Date

July 30, 2021

Package DI Number

00840155408197

Quantity per Package

4

Contains DI Package

00840155408173

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case