Catalog Number

M2300-MG

Brand Name

DeRoyal

Version/Model Number

M2300-MG

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

KMI

Product Code Name

MONITOR, BED PATIENT

Public Device Record Key

38efce3f-ea46-4f79-8335-6781f3ec5fc3

Public Version Date

August 11, 2021

Public Version Number

1

DI Record Publish Date

August 03, 2021

Package DI Number

50749756960620

Quantity per Package

36

Contains DI Package

00749756960625

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case