Catalog Number

-

Brand Name

RebarTM

Version/Model Number

105-5083-153

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

K093750

Product Code

KRA

Product Code Name

Catheter, continuous flush

Public Device Record Key

5be2a0fe-28c1-4057-9853-116caaa0c643

Public Version Date

December 22, 2021

Public Version Number

7

DI Record Publish Date

September 17, 2017

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-