Catalog Number

-

Brand Name

Abena

Version/Model Number

2619

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

January 01, 2023

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

FRO

Product Code Name

Dressing, Wound, Drug

Public Device Record Key

35457703-2b6f-45fd-909e-c4f61b6b25d8

Public Version Date

January 03, 2022

Public Version Number

5

DI Record Publish Date

May 28, 2020

Package DI Number

00190509001865

Quantity per Package

10

Contains DI Package

00190509001742

Package Discontinue Date

January 01, 2022

Package Status

Not in Commercial Distribution

Package Type

Case