Catalog Number

220139

Brand Name

ambIT*

Version/Model Number

220139

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

K162165,K162165,K162165

Product Code

FRN

Product Code Name

Pump, infusion

Public Device Record Key

919a89f7-b3ce-4b57-b887-00321552ef2a

Public Version Date

January 25, 2022

Public Version Number

1

DI Record Publish Date

January 17, 2022

Package DI Number

10193494001084

Quantity per Package

10

Contains DI Package

00193494001087

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

DSP