Catalog Number

-

Brand Name

Rymed

Version/Model Number

415304

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

K093489,K093489,K093489,K093489

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

d3fd8c21-4425-4654-afb8-e09d58ac4fb8

Public Version Date

May 19, 2020

Public Version Number

3

DI Record Publish Date

April 25, 2018

Package DI Number

30817903010705

Quantity per Package

5

Contains DI Package

20817903010708

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case