Catalog Number

69110

Brand Name

Halyard

Version/Model Number

69110

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

FYF

Product Code Name

CAP, SURGICAL

Public Device Record Key

96b9e881-52b6-4ac5-8106-817dd773bb64

Public Version Date

December 22, 2021

Public Version Number

2

DI Record Publish Date

August 31, 2020

Package DI Number

30680651691102

Quantity per Package

3

Contains DI Package

20680651691105

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS