Catalog Number

-

Brand Name

HAEMONETICS ORTHOPAT SYSTEM

Version/Model Number

01500-00

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,K962475

Product Code

CAC

Product Code Name

Apparatus, Autotransfusion

Public Device Record Key

89228290-6e61-4dda-bed2-5e650a5992bf

Public Version Date

January 08, 2021

Public Version Number

4

DI Record Publish Date

June 16, 2017

Package DI Number

30812747017040

Quantity per Package

4

Contains DI Package

20812747017043

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton