Catalog Number

90002

Brand Name

Halyard

Version/Model Number

90002

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

KKX

Product Code Name

Drape, surgical

Public Device Record Key

4caedd47-a68d-45e0-a640-c137d23042ff

Public Version Date

April 07, 2021

Public Version Number

3

DI Record Publish Date

October 07, 2019

Package DI Number

30680651900020

Quantity per Package

36

Contains DI Package

10680651900026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS