Lumenis Pulse 60H, 60Hz

GUDID 07290109144672

LUMENIS LTD.

General/multiple surgical solid-state laser system

• Primary Device ID: 07290109144672
• NIH Device Record Key: bad52847-6fe1-48b4-a1d3-49375cc99631
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lumenis Pulse 60H, 60Hz
• Version Model Number: Lumenis Pulse 60H, 60Hz
• 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	07290109144672 [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: 2022-03-17
• Device Publish Date: 2022-03-09

On-Brand Devices [Lumenis Pulse 60H, 60Hz]

• 07290109144672: Lumenis Pulse 60H, 60Hz
• 07290118853701: Lumenis Pulse 60H, 60Hz