Catalog Number

-

Brand Name

Vasopress

Version/Model Number

VP500DM

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

-

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

K101915,K101915,K101915

Product Code

JOW

Product Code Name

Sleeve, Limb, Compressible

Public Device Record Key

c600f07e-305a-4446-9986-a6759f14b82b

Public Version Date

October 23, 2018

Public Version Number

4

DI Record Publish Date

September 22, 2016

Package DI Number

20815245010080

Quantity per Package

252

Contains DI Package

00815245010062

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Pallet