Catalog Number

-

Brand Name

APEX

Version/Model Number

Domus 3 with 5"+3" Mattress

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

-

Prescription Use (Rx)

-

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FNM

Product Code Name

Mattress, Air Flotation, Alternating Pressure

Public Device Record Key

18274661-2d4e-417b-8310-b7613a895973

Public Version Date

August 06, 2018

Public Version Number

1

DI Record Publish Date

July 04, 2018

Package DI Number

14713025004351

Quantity per Package

2

Contains DI Package

04713025004354

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-