Catalog Number

-

Brand Name

Muc-Away™

Version/Model Number

0492

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

GCX

Product Code Name

Apparatus, Suction, Operating-Room, Wall Vacuum Powered

Public Device Record Key

2b58b0fe-cc8f-4c33-a515-36d758439477

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

May 11, 2017

Package DI Number

10709078003377

Quantity per Package

40

Contains DI Package

00709078003370

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-