Catalog Number

13220

Brand Name

Halyard

Version/Model Number

13220

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

BTR

Product Code Name

Tube, Tracheal (W/Wo Connector)

Public Device Record Key

2856280b-2b63-44b2-9545-a0a2a992cffe

Public Version Date

November 16, 2018

Public Version Number

4

DI Record Publish Date

September 23, 2015

Package DI Number

30680651132209

Quantity per Package

10

Contains DI Package

10680651132205

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-