Catalog Number

-

Brand Name

SUOH 03

Version/Model Number

AHW14R313S

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

-

Product Code

DQX

Product Code Name

WIRE, GUIDE, CATHETER

Public Device Record Key

66ed1e15-a59e-418d-9881-857cf87793dd

Public Version Date

November 22, 2019

Public Version Number

5

DI Record Publish Date

February 10, 2017

Package DI Number

14547327116760

Quantity per Package

5

Contains DI Package

04547327116763

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-