FDA UDI In Commercial Distribution 🇺🇸 United States

Manual Erection System

DI: 04013273001175 · Model: MES 01 · KESSEL medintim GmbH
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Manual Erection System
Primary DI
04013273001175
Version / Model
MES 01
Catalog Number
MES 01
Company Name
KESSEL medintim GmbH
Labeler DUNS
537500365
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-11-19
Public Version
1
Public Version Date
2021-11-29
Public Version Status
New
Public Device Record Key
3735035f-65b9-47a5-924b-98210c1a42d9

Device Description

Vacuum Erection Device for treatment of erectile dysfunction for impotence due to: Diabetes, Protata surgery, elevated blood lipids, vascular diseases, smoking, excessive alcohol

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
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 04013273001175

Customer Contacts

Phone
8008501657