Catalog Number

-

Brand Name

Jelco

Version/Model Number

505011

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

FOZ

Product Code Name

Catheter,intravascular,therapeutic,short-term less than 30 days

Public Device Record Key

72aedaaa-e5e6-4957-9d07-c4bb6549e336

Public Version Date

June 10, 2022

Public Version Number

5

DI Record Publish Date

October 05, 2016

Package DI Number

55019315118607

Quantity per Package

200

Contains DI Package

35019315118603

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CARTON