Catalog Number

47619

Brand Name

Halyard

Version/Model Number

47619

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

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

9fdad69e-d36a-486f-9a1b-9f5a0ccea028

Public Version Date

July 09, 2019

Public Version Number

1

DI Record Publish Date

July 01, 2019

Package DI Number

30680651476198

Quantity per Package

40

Contains DI Package

20680651476191

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS