Lumenis Pulse 120H GA-0008700

GUDID 07290109145464

LUMENIS LTD.

General/multiple surgical solid-state laser system

• Primary Device ID: 07290109145464
• NIH Device Record Key: cda4a96c-493a-4e39-9624-e0ce55f95552
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumenis Pulse 120H
• Version Model Number: Lumenis Pulse 120H
• Catalog Number: GA-0008700
• Company DUNS: 600166524
• Company Name: LUMENIS LTD.
• 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: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx
• Phone: 408-764-3000
• Email: xxx@xxx.xxx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109145464 [Primary]

FDA Product Code

• GEX: Powered Laser Surgical Instrument

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: 2022-08-02
• Device Publish Date: 2022-07-25

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• 07290109145433: Lumenis Pulse 120H
• 07290109145426: Lumenis Pulse 120H
• 07290109145419: Lumenis Pulse 120H
• 07290109145402: Lumenis Pulse 120H
• 07290109145150: Lumenis Pulse Moses 2.0(INT)