Catalog Number

1688

Brand Name

Motion Medical Distributing

Version/Model Number

1688

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

Human Cell, Tissue or Cellular or Tissue-Based Product (HCT/P)

-

FDA Premarket Submission

-

Product Code

OWL

Product Code Name

Peripheral Catheter Insertion Kit

Public Device Record Key

4123701d-3b32-4aca-a602-4b5261a8bc34

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

April 20, 2017

Package DI Number

25060498451448

Quantity per Package

10

Contains DI Package

15060498451441

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case