FDA UDI In Commercial Distribution 🇺🇸 United States

POTENZA

DI: 08800020108395 · Model: Foot Switch · Jeisys Medical Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
POTENZA
Primary DI
08800020108395
Version / Model
Foot Switch
Company Name
Jeisys Medical Inc.
Labeler DUNS
690275362
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-03-16
Public Version
1
Public Version Date
2026-03-24
Public Version Status
New
Public Device Record Key
40aa0d82-c7c6-4eea-8db3-3ec989fad7ae

Device Description

POTENZA Foot Switch

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
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 08800020108395

Premarket Submissions

Submission Number Supplement Number
K192545 000