Catalog Number

KBP1115/B

Brand Name

Bedford™

Version/Model Number

00884450411889

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"

-

For Single-Use

Yes

Prescription Use (Rx)

-

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

a9819c26-9230-4506-8294-8e74a8994864

Public Version Date

February 14, 2020

Public Version Number

1

DI Record Publish Date

February 06, 2020

Package DI Number

10884450411886

Quantity per Package

14

Contains DI Package

00884450411889

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-