Catalog Number

-

Brand Name

neXus

Version/Model Number

130-33-2210

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"

Yes

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

K190160,K190160

Product Code

GEI

Product Code Name

Electrosurgical, Cutting & Coagulation & Accessories

Public Device Record Key

9d5d0a6b-21ff-4395-8566-6084e7747f76

Public Version Date

March 03, 2020

Public Version Number

1

DI Record Publish Date

February 24, 2020

Package DI Number

00841626103429

Quantity per Package

5

Contains DI Package

00841626103122

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

box