Catalog Number

-

Brand Name

Paradym RF

Version/Model Number

VR 9250

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

P980049,P980049,P980049

Product Code

MRM

Product Code Name

DEFIBRILLATOR, IMPLANTABLE, DUAL-CHAMBER

Public Device Record Key

2774b84b-b047-4e4a-b172-6a082beea596

Public Version Date

February 05, 2021

Public Version Number

5

DI Record Publish Date

September 05, 2014

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-