Catalog Number

ADV2308

Brand Name

Advance Plus™ Earloop Procedure Masks

Version/Model Number

ADV2308

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

FXX

Product Code Name

Mask, Surgical

Public Device Record Key

98188259-e1bd-4063-9281-211eae21cab3

Public Version Date

May 06, 2020

Public Version Number

2

DI Record Publish Date

March 10, 2020

Package DI Number

20810012650001

Quantity per Package

10

Contains DI Package

10810012650004

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

case