Catalog Number

-

Brand Name

Giraffe

Version/Model Number

31931

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"

Yes

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

KXJ

Product Code Name

Table, radiologic

Public Device Record Key

620bbe4a-d93d-497f-8c9d-fc42caa86cc4

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

June 28, 2017

Package DI Number

00618125187058

Quantity per Package

7

Contains DI Package

01618125187057

Package Discontinue Date

-

Package Status

-

Package Type

-