Catalog Number

-

Brand Name

Encompass

Version/Model Number

26186-572

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

FRG

Product Code Name

Wrap, sterilization

Public Device Record Key

1ab45130-05aa-4400-adcd-e47f5b6797f0

Public Version Date

November 08, 2019

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

50609953517150

Quantity per Package

24

Contains DI Package

00609953517155

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-