GMPP DCD Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly 7123-CE-0652

GUDID 00817495023229

CANDELA CORPORATION

Dermatological solid-state laser system

• Primary Device ID: 00817495023229
• NIH Device Record Key: 5105b3a1-bbf9-4d89-8e60-b45d111ebb63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GMPP DCD Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly
• Version Model Number: 7123-CE-0652
• Catalog Number: 7123-CE-0652
• 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: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817495023229 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K201111

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: 2022-01-25
• Device Publish Date: 2022-01-17

On-Brand Devices [GMPP DCD Large Spot Option Kit, w/HP, w/SAs, w/Fiber Assembly]

• 00817495023229: 7123-CE-0652
• 00817495024035: GMPP DCD Large Spot