Catalog Number

05-232-010

Brand Name

MABIS

Version/Model Number

05-232-010

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)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K942543,K942543

Product Code

DXN

Product Code Name

System, Measurement, Blood-Pressure, Non-Invasive

Public Device Record Key

d0a1baff-fbd3-4443-a11f-5286fdf27731

Public Version Date

December 14, 2020

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

10767056232010

Quantity per Package

100

Contains DI Package

00767056232013

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton