Catalog Number

-

Brand Name

SourceMark

Version/Model Number

M21302

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

Yes

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

DWJ

Product Code Name

System, Thermal Regulating

Public Device Record Key

39d2a915-5bf2-43d9-a906-5357aa5ea4b8

Public Version Date

December 06, 2021

Public Version Number

2

DI Record Publish Date

July 08, 2020

Package DI Number

10813799004480

Quantity per Package

40

Contains DI Package

00813799004476

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box