Catalog Number

-

Brand Name

Nimbus II Plus

Version/Model Number

Nimbus II Plus

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

K153193,K153193,K153193

Product Code

FRN

Product Code Name

Pump, Infusion

Public Device Record Key

5ad87494-33f8-4cc2-a702-f2f7fa9d98ce

Public Version Date

June 17, 2022

Public Version Number

2

DI Record Publish Date

March 06, 2019

Package DI Number

20817170020165

Quantity per Package

60

Contains DI Package

00817170020161

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Case