Catalog Number

-

Brand Name

Halyard

Version/Model Number

48531

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

K180139,K180139,K180139

Product Code

FRG

Product Code Name

Wrap, sterilization

Public Device Record Key

d478cb36-4ce3-4d89-80cb-cb2b68156730

Public Version Date

June 15, 2020

Public Version Number

2

DI Record Publish Date

May 20, 2020

Package DI Number

30885632243886

Quantity per Package

2

Contains DI Package

10885632243882

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-