Catalog Number

AS-05500

Brand Name

ARROW

Version/Model Number

IPN040061

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

K103658,K103658,K103658

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

afe8b082-a38c-4a39-aec8-d91967297e5e

Public Version Date

July 01, 2022

Public Version Number

6

DI Record Publish Date

December 22, 2016

Package DI Number

20801902126140

Quantity per Package

25

Contains DI Package

50801902126141

Package Discontinue Date

June 29, 2022

Package Status

Not in Commercial Distribution

Package Type

Box