Catalog Number

83070-22

Brand Name

Temena

Version/Model Number

83070-22

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)

-

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

GXZ

Product Code Name

Electrode, Needle

Public Device Record Key

feb7cf47-0f73-4355-b219-4721f49bad7d

Public Version Date

March 29, 2018

Public Version Number

2

DI Record Publish Date

November 20, 2017

Package DI Number

03700339702527

Quantity per Package

10

Contains DI Package

03700339713356

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

Box