Catalog Number

-

Brand Name

NICO BrainPath

Version/Model Number

NN-8024

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)

Yes

Over the Counter (OTC)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GDG

Product Code Name

Hook, Surgical, General & Plastic Surgery

Public Device Record Key

ecd7b0e4-0d5b-4c45-a9c1-c92c8404105c

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

September 14, 2016

Package DI Number

10816744028241

Quantity per Package

2

Contains DI Package

00816744028244

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-