Jeisys Medical Inc.

GUDID 08800020106407

ALPHA Tip

Jeisys Medical Inc.

Radio-frequency skin/body contouring system

• Primary Device ID: 08800020106407
• NIH Device Record Key: 790f0d15-18d9-46b4-b8b8-81a17601ddbb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jeisys Medical Inc.
• Version Model Number: ALPHA Tip
• Company DUNS: 690275362
• Company Name: Jeisys Medical Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800020106407 [Primary]

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: 2025-09-02
• Device Publish Date: 2025-08-25

On-Brand Devices [Jeisys Medical Inc.]

• 08800020106407: ALPHA Tip
• 08800020106759: DENSITY Noir Main body