Lumenis Pulse, Moses 2.0 (INT) GA-0006902D

GUDID 07290109147208

LUMENIS LTD.

General/multiple surgical solid-state laser system

• Primary Device ID: 07290109147208
• NIH Device Record Key: 42d1cf02-db22-43f3-894c-0cdcde6429a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumenis Pulse, Moses 2.0 (INT)
• Version Model Number: Lumenis Pulse, Moses 2.0 (INT)
• Catalog Number: GA-0006902D
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109147208 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-02-26
• Device Publish Date: 2022-09-18

Devices Manufactured by LUMENIS LTD.

• 07290109147161 - Lumenis Pulse 120H: 2025-02-26
• 07290109147178 - Lumenis Pulse 120H: 2025-02-26
• 07290109147185 - Lumenis Pulse, Moses 2.0 (DOM): 2025-02-26
• 07290109147192 - Lumenis Pulse 120H: 2025-02-26
• 07290109147208 - Lumenis Pulse, Moses 2.0 (INT): 2025-02-26
• 07290109147208 - Lumenis Pulse, Moses 2.0 (INT): 2025-02-26
• 07290109147215 - Lumenis Pulse 120H: 2025-02-26
• 07290109147222 - Lumenis Pulse 120H: 2025-02-26
• 07290109147291 - Lumenis Pulse 120H: 2025-02-26