POTENZA

GUDID 08800020101525

POTENZA Neutral Electrode Pad Cable

Jeisys Medical Inc.

Electrosurgical system

• Primary Device ID: 08800020101525
• NIH Device Record Key: aaf69e43-6bdc-4340-bc7e-2009acb42015
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: POTENZA
• Version Model Number: Neutral Electrode Pad Cable
• Company DUNS: 690275362
• Company Name: Jeisys Medical Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800020101525 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K192545

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-24
• Device Publish Date: 2026-03-16

On-Brand Devices [POTENZA]

• 08800020111012: Fractional RF Microneedle System
• 08800020108425: POTENZA Handpiece Stand
• 08800020108401: POTENZA Power Cable
• 08800020108395: POTENZA Foot Switch
• 08800020101525: POTENZA Neutral Electrode Pad Cable