Catalog Number

-

Brand Name

Nimbus

Version/Model Number

Nimbus

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FRN

Product Code Name

Pump, Infusion

Public Device Record Key

86196cae-3c1d-447a-8c75-70e4b429aa87

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

September 23, 2016

Package DI Number

10817170020007

Quantity per Package

24

Contains DI Package

00817170020000

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-