Catalog Number

-

Brand Name

MTG Jiffy Cath™

Version/Model Number

20116

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

K080878,K080878,K080878

Product Code

KOD

Product Code Name

Catheter, Urological

Public Device Record Key

b6ff677b-e340-41c7-89d4-70a7ce79fd53

Public Version Date

September 18, 2019

Public Version Number

1

DI Record Publish Date

September 10, 2019

Package DI Number

10851593006804

Quantity per Package

4

Contains DI Package

20851593006801

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-