Catalog Number

-

Brand Name

NICO Myriad

Version/Model Number

NN-8000

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

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

0c9f8ee3-42f5-470a-92a6-6a40948077b9

Public Version Date

April 09, 2019

Public Version Number

3

DI Record Publish Date

September 14, 2016

Package DI Number

10816744028005

Quantity per Package

3

Contains DI Package

00816744028008

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-