Catalog Number

A909216M

Brand Name

SureStep™ Foley Tray System Lubri-Sil® Temperature Sensing Foley Catheter

Version/Model Number

A909216M

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Conditional

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

Yes

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

-

FDA Premarket Submission

-

Product Code

EZL

Product Code Name

CATHETER, RETENTION TYPE, BALLOON

Public Device Record Key

a7c38cfa-a6f2-4ae2-ab12-7e49b2255a1f

Public Version Date

December 04, 2020

Public Version Number

3

DI Record Publish Date

December 08, 2015

Package DI Number

10801741104760

Quantity per Package

10

Contains DI Package

00801741104763

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CA