Catalog Number

M17-0000-0000

Brand Name

Medviron Bassinet

Version/Model Number

Traverse Bay Bassinet 1 Drawer

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

NZG

Product Code Name

Bassinet, Hospital

Public Device Record Key

10c0b3c3-2ed5-4f28-ae1b-5b885d8ac229

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

October 04, 2016

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-