Catalog Number

Not Applicable

Brand Name

MedSource Patient Mover

Version/Model Number

MS-95202

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

FMR

Product Code Name

Device, Transfer, Patient, Manual

Public Device Record Key

672c299e-1b19-4425-8c76-c99f96b631bd

Public Version Date

March 25, 2022

Public Version Number

2

DI Record Publish Date

July 26, 2021

Package DI Number

00840155405950

Quantity per Package

1

Contains DI Package

00840155412507

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case