Catalog Number

ASK-05060-CHO

Brand Name

ARROW

Version/Model Number

IPN040106

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

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

dcc5c70b-07ad-473e-8edb-cdc5e86bff86

Public Version Date

January 08, 2021

Public Version Number

5

DI Record Publish Date

September 16, 2016

Package DI Number

30801902073854

Quantity per Package

5

Contains DI Package

00801902073853

Package Discontinue Date

July 20, 2018

Package Status

Not in Commercial Distribution

Package Type

Box