Catalog Number

393059

Brand Name

Itrevia 5 VR-T

Version/Model Number

393059

Device Commercial Distribution Status

Not in Commercial Distribution

Commercial Distribution End Date

October 07, 2020

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

LWS

Product Code Name

Implantable cardioverter defibrillator (non-CRT)

Public Device Record Key

491cdd28-6880-4b2c-9735-0fc6954f1e5f

Public Version Date

February 05, 2021

Public Version Number

6

DI Record Publish Date

February 18, 2015

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-