FDA UDI In Commercial Distribution 🇺🇸 United States

Active3 Erection System

DI: 04013273001915 · Model: AES 3 · KESSEL medintim GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Active3 Erection System
Primary DI
04013273001915
Version / Model
AES 3
Catalog Number
AES 3
Company Name
KESSEL medintim GmbH
Labeler DUNS
537500365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-01-29
Public Version
1
Public Version Date
2020-02-06
Public Version Status
New
Public Device Record Key
ba0587af-4d85-41d3-9527-40bf632fda02

Device Description

Vaccum Erection Device for treatment of erectily dysfunction

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
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
No
Has Expiration Date
No
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 04013273001915

Customer Contacts

Storage Conditions

Type
Handling Environment Temperature
Temperature Range
-25 – 70 Degrees Celsius