Catalog Number

213-013

Brand Name

Surge Cardiovascular

Version/Model Number

213-013

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

GEJ

Product Code Name

Carrier, Ligature

Public Device Record Key

923ea2cf-c360-48fa-9b4e-723f68eff042

Public Version Date

September 21, 2022

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

10817278010023

Quantity per Package

4

Contains DI Package

00817278010026

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case