Catalog Number

AB-17040-N

Brand Name

ARROW

Version/Model Number

IPN040015

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

K121403,K121403,K121403

Product Code

CAZ

Product Code Name

Anesthesia conduction kit

Public Device Record Key

5ccf4b65-8277-4d1c-8756-f6cc0e8b7c9d

Public Version Date

February 27, 2020

Public Version Number

6

DI Record Publish Date

January 10, 2017

Package DI Number

10801902033168

Quantity per Package

10

Contains DI Package

40801902033169

Package Discontinue Date

February 24, 2020

Package Status

Not in Commercial Distribution

Package Type

Box