Synergy™ Ablation System A000423

GUDID 00818354016291

Glidepath Tape (1-Unit)

ATRICURE, INC.

Cardiac ablation system applicator introducer/sizer

• Primary Device ID: 00818354016291
• NIH Device Record Key: dbd134ed-d0d2-4e5f-b0a9-97fef23cb90c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Synergy™ Ablation System
• Version Model Number: GPT300
• Catalog Number: A000423
• Company DUNS: 006133784
• Company Name: ATRICURE, 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00818354016291 [Primary]

FDA Product Code

• FZX: Guide, Surgical, Instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-12-13
• Device Publish Date: 2018-11-12

On-Brand Devices [Synergy™ Ablation System]

• 00818354016291: Glidepath Tape (1-Unit)
• 00818354010718: Glidepath Tape (3-Unit)
• 00818354010596: AtriCure Switch Box
• 00818354010558: Isolator Synergy™ Surgical Ablation System Open, Short Jaw, Left Curve
• 00818354010503: Isolator Synergy™ Surgical Ablation System Open, Long Jaw, Left Curve
• 00818354010206: Ablation and Sensing Unit
• 00818354010312: Footswitch ASU2/ASU3
• 30840143902318: Isolator Synergy™ Surgical Ablation System Open, Short Jaw, Left Curve
• 30840143902141: Isolator Synergy™ Surgical Ablation System Open, Long Jaw, Left Curve
• 30840143903018: AtriCure Switch Box
• 30840143901625: Glidepath Tape (3-Unit)