Catalog Number

Q21214-19021

Brand Name

PEDIATRIC ULTRA FLEX®

Version/Model Number

Q21214-19021

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

-

Product Code

CAI

Product Code Name

Circuit, breathing (w connector, adaptor, y piece)

Public Device Record Key

e8a165bf-0d50-4def-8aeb-c6c96fb0f2a8

Public Version Date

October 24, 2022

Public Version Number

2

DI Record Publish Date

August 27, 2020

Package DI Number

00612649215105

Quantity per Package

20

Contains DI Package

00612649215112

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-