FDA UDI Not in Commercial Distribution 🇺🇸 United States

Active Erection System

DI: 04013273000116 · Model: AES 01 · KESSEL medintim GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Active Erection System
Primary DI
04013273000116
Version / Model
AES 01
Company Name
KESSEL medintim GmbH
Labeler DUNS
537500365
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-01-21
Public Version
3
Public Version Date
2023-08-16
Public Version Status
Update
Public Device Record Key
61d5a9bc-a299-4135-b7c9-5dddeec3fce3
Distribution End Date
2023-08-16

Device Description

Vacuum Erection Device for treatment of erectile dysfunction

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
Yes
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
LKY Device, External Penile Rigidity

GMDN Terms

Code Name
17744 Penile vacuum device

Identifiers

Type ID
Primary 04013273000116

Customer Contacts