Catalog Number

48737

Brand Name

Nova

Version/Model Number

SUREFLEX

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

Yes

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

NBW

Product Code Name

SYSTEM, TEST, BLOOD GLUCOSE, OVER THE COUNTER

Public Device Record Key

1b24b88e-8768-47fb-9695-652f1ea7c733

Public Version Date

August 09, 2019

Public Version Number

3

DI Record Publish Date

September 20, 2016

Package DI Number

10385480487372

Quantity per Package

20

Contains DI Package

00385480487375

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Carton