Catalog Number

HN1-40

Brand Name

AVANOS

Version/Model Number

39203

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

BSP

Product Code Name

NEEDLE, CONDUCTION, ANESTHETIC (W/WO INTRODUCER)

Public Device Record Key

4ae8ccfe-ac16-4d71-a55a-a98b2aae2a66

Public Version Date

January 08, 2021

Public Version Number

3

DI Record Publish Date

July 03, 2020

Package DI Number

10193494392038

Quantity per Package

10

Contains DI Package

00193494392031

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS