Catalog Number

173810-000240

Brand Name

RUSCH

Version/Model Number

IPN915206

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

80c33550-046f-4aa5-8b0c-56f588ccae5b

Public Version Date

December 04, 2020

Public Version Number

3

DI Record Publish Date

February 06, 2020

Package DI Number

24026704710915

Quantity per Package

72

Contains DI Package

04026704710911

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton