Catalog Number

76094-ACM5059

Brand Name

Halyard

Version/Model Number

05059

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

PUI

Product Code Name

Drape, Surgical, Exempt

Public Device Record Key

7fe3c9e2-1e76-4f26-9b41-19064d697efa

Public Version Date

December 22, 2021

Public Version Number

8

DI Record Publish Date

September 30, 2016

Package DI Number

30680651050596

Quantity per Package

8

Contains DI Package

10680651050592

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS