Catalog Number

181225

Brand Name

Halyard

Version/Model Number

93162

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

April 14, 2018

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

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

c3d26951-d399-4335-9118-2f157c2215ea

Public Version Date

December 13, 2021

Public Version Number

6

DI Record Publish Date

January 31, 2016

Package DI Number

30609038161267

Quantity per Package

10

Contains DI Package

10609038161263

Package Discontinue Date

April 14, 2018

Package Status

Not in Commercial Distribution

Package Type

CS