Synergy™ Ablation System

Basic Information

• Brand Name: Synergy™ Ablation System
• Primary DI: 00818354010718
• Version / Model: GPT300
• Catalog Number: A000437
• Company Name: ATRICURE, INC.
• Labeler DUNS: 006133784
• Distribution Status: In Commercial Distribution
• Device Count in Pkg: 1
• Record Status: Published
• Publish Date: 2018-11-12
• Public Version: 1
• Public Version Date: 2018-12-13
• Public Version Status: New
• Public Device Record Key: b91a5a9a-59a9-4004-940d-2e27614114c1

Device Description

Glidepath Tape (3-Unit)

Device Characteristics

• Single Use: Yes
• Prescription Use (Rx): Yes
• Over the Counter (OTC): No
• Kit: No
• Combination Product: No
• HCT/P: No
• Contains NRL: No
• Not Made with NRL: Yes
• MRI Safety: Labeling does not contain MRI Safety Information
• Direct Marking Exempt: No
• PM Exempt: No
• Has Serial Number: No
• Has Lot/Batch Number: Yes
• Has Manufacturing Date: No
• Has Expiration Date: Yes
• Has Donation ID: No

Sterilization

• Is Sterile: Yes
• Sterilization Prior Use: No

Product Codes

Code	Name	Medical Specialty	Regulation #	Device Class
FZX	Guide, Surgical, Instrument	General, Plastic Surgery	878.4800	1

GMDN Terms

Code	Name	Definition	Implantable	Status
45454	Cardiac ablation system applicator introducer/sizer	A sterile, flexible device that is used to determine the appropriate size of a cardiac tissue ablation system applicator [to determine the appropriate number of transducers (ablation cells) required to treat the target tissue] and/or used to introduce and guide it into position, or used to help fix the applicator in position. It is designed as a highly flexible tubular-like device with markings indicating different applicator sizes and shaped to facilitate introduction into the pericardium, or may be flexible tubes with hooked ends and wires to fasten an applicator. This is a single-use device.	No	Active

Identifiers

Type	ID	Issuing Agency	Package Type	Qty per Pkg	Pkg Status	Pkg Discontinue Date
Primary	00818354010718	GS1