PRO Series Fiber Assembly

GUDID 00817495025179

Fiber Assembly

Candela Corporation

Dermatological laser beam producing handpiece

• Primary Device ID: 00817495025179
• NIH Device Record Key: 9330765e-d955-4973-9cc1-f909d92ccf37
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRO Series Fiber Assembly
• Version Model Number: 7122-00-9419
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00817495025179 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-07-07
• Device Publish Date: 2023-06-29

On-Brand Devices [PRO Series Fiber Assembly]

• 00817495021157: Fiber Assembly
• 00817495025179: Fiber Assembly
• 00817495025148: Fiber Assembly
• 00817495023908: Fiber Assembly