Glase Pro U Laser System

GUDID 00817495023557

Glase Pro U Laser System

Candela Corporation

Dermatological solid-state laser system

• Primary Device ID: 00817495023557
• NIH Device Record Key: dedb20cd-ec46-4f03-97ec-7b0efc7220a7
• Commercial Distribution Discontinuation: 2024-10-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Glase Pro U Laser System
• Version Model Number: 9914-CH-9030
• Company DUNS: 053468385
• Company Name: Candela Corporation
• 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: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com
• Phone: 800-735-2737
• Email: customerservice@syneron-candela.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817495023557 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140732

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: 2024-10-15
• Device Publish Date: 2022-12-16

On-Brand Devices [Glase Pro U Laser System]

• 00817495024646: Glase Pro U Laser System
• 00817495023557: Glase Pro U Laser System