Catalog Number

-

Brand Name

ORTHO CONNECT

Version/Model Number

2.0

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

BK160124

Product Code

KSZ

Product Code Name

System, Test, Automated Blood Grouping And Antibody

Public Device Record Key

cee737c5-7245-4978-b8b1-da6d4a4d48e6

Public Version Date

November 16, 2020

Public Version Number

2

DI Record Publish Date

October 02, 2018

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-