Catalog Number

-

Brand Name

Veridian

Version/Model Number

09-183SL

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

72a16f82-4a70-4b5d-9db9-2677b0c16a04

Public Version Date

December 04, 2020

Public Version Number

2

DI Record Publish Date

May 08, 2019

Package DI Number

10845717009475

Quantity per Package

24

Contains DI Package

00845717009478

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Master Carton