Catalog Number

-

Brand Name

Up & Up

Version/Model Number

PC40-TG

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

FLL

Product Code Name

Thermometer, Electronic, Clinical

Public Device Record Key

efa1d591-7289-44d6-9e7c-7c72dbd47999

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 02, 2016

Package DI Number

20642632760408

Quantity per Package

48

Contains DI Package

10642632760401

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box packing