Catalog Number

QUE2150

Brand Name

Aero-Med

Version/Model Number

QUE2150

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)

-

Over the Counter (OTC)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LRP

Product Code Name

TRAY, SURGICAL

Public Device Record Key

92818a8b-b1fc-4109-a8da-548160631c51

Public Version Date

June 17, 2022

Public Version Number

3

DI Record Publish Date

August 15, 2019

Package DI Number

50810010892329

Quantity per Package

100

Contains DI Package

00810010892324

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

CASE