Catalog Number

MS760FS

Brand Name

MedStream

Version/Model Number

MS760FS

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

Yes

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

-

FDA Premarket Submission

-

Product Code

FPA

Product Code Name

Set, Administration, Intravascular

Public Device Record Key

cd0d4499-2115-4d5d-b1dd-3ea0f06b2425

Public Version Date

April 07, 2021

Public Version Number

4

DI Record Publish Date

September 23, 2016

Package DI Number

20842472102714

Quantity per Package

6

Contains DI Package

10842472102717

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-