Catalog Number

5875-15

Brand Name

PAD, FOAM, DISPOSABLE POST

Version/Model Number

5875-12

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FMP

Product Code Name

Protector, Skin Pressure

Public Device Record Key

81f023ab-c51f-4da7-87a6-0b946aa2c72a

Public Version Date

August 09, 2021

Public Version Number

1

DI Record Publish Date

July 30, 2021

Package DI Number

10842430111751

Quantity per Package

3

Contains DI Package

00842430111754

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

multi-pack