Catalog Number

AB-19604-S

Brand Name

ARROW

Version/Model Number

IPN040031

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"

Yes

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

54b1ed1e-7860-4ef1-bdc2-931c5679ea88

Public Version Date

July 22, 2019

Public Version Number

3

DI Record Publish Date

September 01, 2017

Package DI Number

30801902126048

Quantity per Package

10

Contains DI Package

20801902126041

Package Discontinue Date

February 02, 2018

Package Status

Not in Commercial Distribution

Package Type

Case