Emerge

GUDID 00841494100179

Emerge Laser Assembly

Cynosure, Inc.

Dermatological diode laser system

• Primary Device ID: 00841494100179
• NIH Device Record Key: 816dbca9-1003-4acd-a312-8cdb11863148
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Emerge
• Version Model Number: 0500-0001
• Company DUNS: 780318028
• Company Name: Cynosure, Inc.
• 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	00841494100179 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K111840

FDA Product Code

• ONG: Powered laser surgical instrument with microbeam\fractional output

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: 2018-07-06
• Device Publish Date: 2016-09-24

On-Brand Devices [Emerge]

• 00841494100629: Emerge remanufactured
• 00841494100179: Emerge Laser Assembly