Catalog Number

-

Brand Name

Medquip

Version/Model Number

MQ0911

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

September 29, 2019

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

-

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

BTI

Product Code Name

Compressor, air, portable

Public Device Record Key

248e72f3-b956-4890-86e0-7bc353567d15

Public Version Date

June 10, 2022

Public Version Number

4

DI Record Publish Date

September 28, 2016

Package DI Number

50718122220392

Quantity per Package

6

Contains DI Package

00718122220397

Package Discontinue Date

June 21, 2019

Package Status

Not in Commercial Distribution

Package Type

-