Surgi-Max™ JSM120IEC

GUDID 04250337120001

joimax Endovapor®/Surgi-Max® Dual Radio-Frequency

Joimax GmbH

Electrosurgical system

• Primary Device ID: 04250337120001
• NIH Device Record Key: 36a624af-a866-4d77-96c2-73cb3a6d24fd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Surgi-Max™
• Version Model Number: JSM120IEC
• Catalog Number: JSM120IEC
• Company DUNS: 344267187
• Company Name: Joimax GmbH
• 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: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com
• Phone: +497212551407010
• Email: info@joimax.com

Device Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04250337120001 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K170358

FDA Product Code

• GEI: Electrosurgical, cutting & coagulation & accessories

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2023-04-04
• Device Publish Date: 2022-12-30

On-Brand Devices [Surgi-Max™]

• 04250337120063: Surgi-Max™ Disposable Trigger-Flex™
• 04250337120032: Surgi-Max™ Disposable Trigger-Flex™
• 04250337120025: Neutral Plate, reusable for Surgi-Max®
• 04250337120018: Surgi-Max™ Disposable Trigger-Flex™
• 04250337120001: joimax Endovapor®/Surgi-Max® Dual Radio-Frequency
• 04250337105398: Endovapor®/Surgi-Max® Footswitch