Catalog Number

2700-23-EN

Brand Name

SteriPath Gen2, 23G

Version/Model Number

2700-23-EN

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

K192247,K192247

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

02134884-ff15-44d4-990b-038a3bf1106d

Public Version Date

January 06, 2022

Public Version Number

4

DI Record Publish Date

November 06, 2020

Package DI Number

10858366007020

Quantity per Package

10

Contains DI Package

00858366007023

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Sales Pack