Catalog Number

-

Brand Name

Gesiva Medical

Version/Model Number

Medium High Tension Ring

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In HIBCC

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

-

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

52ec4683-f49c-44eb-bce5-10f6c780cf0b

Public Version Date

April 27, 2018

Public Version Number

3

DI Record Publish Date

January 09, 2018

Package DI Number

B598GMMHT0002

Quantity per Package

2

Contains DI Package

B598GMMHT0001

Package Discontinue Date

-

Package Status

In Commercial Distribution

Package Type

-