Slimline™ EZ SIS 365 0644-018-01

GUDID 07290109147031

LUMENIS LTD.

General/multiple surgical laser system beam guide, single-use

• Primary Device ID: 07290109147031
• NIH Device Record Key: f4876415-3d8f-4727-9fc0-ac46df83adfe
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Slimline™ EZ SIS 365
• Version Model Number: Slimline™ EZ SIS 365
• Catalog Number: 0644-018-01
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• 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	07290109147031 [Primary]
GS1	17290109147038 [Package]; Package: [3 Units]; In Commercial Distribution

FDA Product Code

• GEX: Powered Laser Surgical Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-09-12
• Device Publish Date: 2022-09-04

Devices Manufactured by LUMENIS LTD.

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• 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