Stellar SapphireCool LG 15x35

GUDID 07290109144931

LUMENIS LTD.

Multi-modality skin surface treatment system

• Primary Device ID: 07290109144931
• NIH Device Record Key: f0673034-a064-406c-8ec6-d22f0d58974e
• Commercial Distribution Discontinuation: 2023-08-10
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Stellar SapphireCool LG 15x35
• Version Model Number: Stellar SapphireCool LG 15x35
• 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: true
• Serial Number: false
• 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: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com
• Phone: +97249599000
• Email: info@lumenis.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290109144931 [Primary]

FDA Product Code

• ONF: Powered Light Based Non-Laser Surgical Instrument With Thermal Effect

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2023-08-16
• Device Publish Date: 2019-08-06

Devices Manufactured by LUMENIS LTD.

• 07290118853701 - Lumenis Pulse 60H, 60Hz: 2023-12-18
• 07290109144924 - Stellar SapphireCool LG 6mm: 2023-08-16
• 07290109144931 - Stellar SapphireCool LG 15x35: 2023-08-16
• 07290109144931 - Stellar SapphireCool LG 15x35: 2023-08-16
• 07290109144948 - Stellar SapphireCool LG 8x15: 2023-08-16
• 07290109146676 - SurgiTouch Scanner: 2022-09-30
• 07290109146133 - UltraPulse® DUO: 2022-09-28 UltraPulse DUO
• 07290109147055 - VersaPulse PowerSuite 80/100W: 2022-09-27
• 07290109147062 - VersaPulse PowerSuite 80/100W: 2022-09-27