Catalog Number

-

Brand Name

Encompass

Version/Model Number

CD0903

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

-

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

KKX

Product Code Name

Drape, surgical

Public Device Record Key

7e9afd6e-97bd-48b9-988b-5b716ac62bfb

Public Version Date

February 05, 2021

Public Version Number

4

DI Record Publish Date

September 18, 2016

Package DI Number

50609953271090

Quantity per Package

72

Contains DI Package

00609953271095

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-