Catalog Number

-

Brand Name

Meridian Medical

Version/Model Number

#6002

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 01, 2019

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

JOW

Product Code Name

Sleeve, Limb, Compressible

Public Device Record Key

991ee20c-4e44-4cda-98c4-c7d5ed3d9688

Public Version Date

August 20, 2019

Public Version Number

3

DI Record Publish Date

October 19, 2016

Package DI Number

30815067040118

Quantity per Package

20

Contains DI Package

00815067040117

Package Discontinue Date

April 01, 2019

Package Status

Not in Commercial Distribution

Package Type

CA