Catalog Number

ASK-04001-VM1

Brand Name

ARROW

Version/Model Number

IPN922609

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

f7054498-49d6-4993-a1c7-fd42b0b7bd45

Public Version Date

August 09, 2021

Public Version Number

1

DI Record Publish Date

July 30, 2021

Package DI Number

20801902202110

Quantity per Package

1

Contains DI Package

10801902202113

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case