Catalog Number

SANOCBTCRA

Brand Name

CARDINAL HEALTH

Version/Model Number

SANOCBTCRA

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

GAA

Product Code Name

NEEDLE, ASPIRATION AND INJECTION, DISPOSABLE

Public Device Record Key

4d945f7c-a3e0-4d9c-a2df-f1a028f1da8d

Public Version Date

June 17, 2022

Public Version Number

5

DI Record Publish Date

April 04, 2017

Package DI Number

50887488690962

Quantity per Package

8

Contains DI Package

10887488690964

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE