Catalog Number

-

Brand Name

HAEMONETICS ORTHOPAT & CARDIOPAT SYSTEMS

Version/Model Number

01200-00

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

Yes

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

K962475,K962475

Product Code

CAC

Product Code Name

Apparatus, Autotransfusion

Public Device Record Key

ab426d7e-0305-402e-a62f-ca76ff094768

Public Version Date

January 08, 2021

Public Version Number

4

DI Record Publish Date

September 24, 2015

Package DI Number

30812747017026

Quantity per Package

40

Contains DI Package

10812747017022

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton