Catalog Number

-

Brand Name

PRIUS

Version/Model Number

FC-PHR0041

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

72967ee6-e0df-4330-ab0e-9dd2266f037c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 25, 2016

Package DI Number

24717677480041

Quantity per Package

2

Contains DI Package

04717677480047

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

BOX