Catalog Number

-

Brand Name

McKesson

Version/Model Number

16-SLFOL3012

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"

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

-

Product Code

EZL

Product Code Name

Catheter, Retention Type, Balloon

Public Device Record Key

25f6f24f-7cc7-48ff-b13c-79d7eb89d076

Public Version Date

December 04, 2020

Public Version Number

3

DI Record Publish Date

January 06, 2020

Package DI Number

40612479245608

Quantity per Package

20

Contains DI Package

20612479245598

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case