Catalog Number

5SDVUMHRTWAA

Brand Name

Getinge 500 Series

Version/Model Number

533HC

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

K122071

Product Code

FLE

Product Code Name

Sterilizer, Steam

Public Device Record Key

497dcafe-bb18-4fba-ab38-72b561d339b0

Public Version Date

March 02, 2020

Public Version Number

1

DI Record Publish Date

February 21, 2020

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-