Catalog Number

46091-52

Brand Name

ICU Medical

Version/Model Number

46091-52

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"

Yes

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

K061573,K061573

Product Code

DRS

Product Code Name

Transducer, blood-pressure, extravascular

Public Device Record Key

ca41e2eb-b613-4860-82ec-3cd63323287d

Public Version Date

October 26, 2021

Public Version Number

2

DI Record Publish Date

August 29, 2021

Package DI Number

10840619069022

Quantity per Package

25

Contains DI Package

00840619069025

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CS