Active Erection System - Vacuum Erection Device for treatment of erectile - KESSEL medintim GmbH

Duns Number:537500365

Device Description: Vacuum Erection Device for treatment of erectile dysfunction

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More Product Details

Catalog Number

-

Brand Name

Active Erection System

Version/Model Number

AES 01

Device Commercial Distribution Status

In Commercial Distribution

Commercial Distribution End Date

-

Issuing Agency

In GS1

Product Characteristics

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 Details

Product Code

LKY

Product Code Name

Device, External Penile Rigidity

Device Record Status

Public Device Record Key

61d5a9bc-a299-4135-b7c9-5dddeec3fce3

Public Version Date

February 21, 2019

Public Version Number

1

DI Record Publish Date

January 21, 2019

Additional Identifiers

Package DI Number

None

Quantity per Package

-

Contains DI Package

-

Package Discontinue Date

-

Package Status

-

Package Type

-

"KESSEL MEDINTIM GMBH" Characteristics
Device Class Device Class Description No of Devices
2 A medical device with a moderate to high risk that requires special controls. 9