Catalog Number

VX-V7-D

Brand Name

Vaxaid

Version/Model Number

Vaxaid V7 Delux

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)

Yes

Kit

-

Combination Product

-

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

-

FDA Premarket Submission

-

Product Code

LKY

Product Code Name

Device, External Penile Rigidity

Public Device Record Key

d6098009-9046-4aaa-b6e2-2a09f6c9c728

Public Version Date

July 13, 2021

Public Version Number

2

DI Record Publish Date

March 01, 2019

Package DI Number

05060140208495

Quantity per Package

10

Contains DI Package

05060140208488

Package Discontinue Date

July 12, 2021

Package Status

Not in Commercial Distribution

Package Type

Box