Catalog Number

-

Brand Name

up&up

Version/Model Number

MT16I2-TG (245-03-1093)

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

573b8aab-8684-4a1e-b427-d80510c2ee0c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

March 21, 2017

Package DI Number

20642632760255

Quantity per Package

12

Contains DI Package

10642632760258

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box packing