Catalog Number

1731-A

Brand Name

1731-A Standard Crib

Version/Model Number

1731-A

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)

Yes

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

a5a74930-cc49-47b1-863f-edb9a41f0dc2

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

March 17, 2017

Package DI Number

00856402007006

Quantity per Package

1

Contains DI Package

00852231007996

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-