Catalog Number

FL36

Brand Name

ook snow MH

Version/Model Number

FL36 ook snow MH

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

MRI safety Status

MR Unsafe

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

FNL

Product Code Name

Bed, Ac-Powered Adjustable Hospital

Public Device Record Key

6a96709b-46d0-4778-98d3-98050340adb4

Public Version Date

December 24, 2018

Public Version Number

1

DI Record Publish Date

November 21, 2018

Package DI Number

10670482000163

Quantity per Package

1

Contains DI Package

00670482000166

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-