Home GUDID 30840143913703 Multifunctional Ablation Generator
Primary DI 30840143913703
Brand Multifunctional Ablation Generator
Company ATRICURE, INC.
Model MAG
Catalog number A001372
Device description The MAG Generator Unit is intended to transmit radiofrequency (RF) energy to the electrodes of AtriCure RF ablation handheld devices.
Published 2026-05-27
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use false Product Codes# Code, Name table Code Name OCM Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class OCM Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation Unknown 3
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 10840143913709 Direct Marking GS1 0 30840143913703 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 10840143913709 10840143913709 30840143913703 30840143913703
GMDN Terms# Term, Definition table Term Definition Cardiac radio-frequency ablation system generator An electrically-powered, noninvasive device intended to be used to generate radio-frequency energy to create ablative lesions in the cardiac tissue of a beating heart in the treatment of cardiac arrhythmias. The generator includes controls and may include electrocardiograph (ECG) interfacing/monitoring functionality. It may be intended to be used with a radio-frequency catheter for endocardial ablation and/or an epicardial probe for epicardial ablation.
Storage And Handling# Type, Low, High table Type Low High Condition Handling Environment Humidity 0 0 Handling Environment Temperature 0 0 Storage Environment Humidity 0 0 Storage Environment Temperature 0 0
Sterilization Methods# Method table Method High-level Disinfectant
Regulatory Flags# DUNS number 006133784 Device count 1 DM exempt false Premarket exempt false HCT/P false Kit false Combination product false Lot or batch false Serial number true Manufacturing date on label true Expiration date on label false Donation ID number false Contains natural rubber latex false No natural rubber latex true Sterilization required before use true Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 10840143902666 cryoICE® System A001150 A001150-1 2026-05-27 10840143902673 cryoICE® System A001150 A001150-2 2026-05-27 10840143902680 cryoICE® System A001150 A001150-3 2026-05-27 10840143902697 cryoICE® System A001150 A001150-4 2026-05-27 10840143902703 cryoICE® System A001150 A001150-5 2026-05-27 10840143902710 cryoICE® System A001150 A001150-6 2026-05-27 10840143902727 cryoICE® System A001150 A001150-7 2026-05-27 10840143902734 cryoICE® System A001150 A001150-8 2026-05-27 30840143904343 cryoICE® System CMF1 A001359 2026-05-27 30840143912164 AtriCure® cryoICE® BOX ACM1 A000896-5 2026-05-27 10840143913761 Isolator Synergy™ OSL2 A000432-12 2026-05-12 10840143913440 AtriClip PRO® Gillinov-Cosgrove™ LAA Exclusion System PRO135 A000824 2026-04-28 10840143913457 AtriClip PRO® Gillinov-Cosgrove™ LAA Exclusion System PRO140 A000825 2026-04-28 10840143913464 AtriClip PRO® Gillinov-Cosgrove™ LAA Exclusion System PRO145 A000826 2026-04-28 10840143913471 AtriClip PRO® Gillinov-Cosgrove™ LAA Exclusion System PRO150 A000827 2026-04-28 10840143913488 AtriClip PRO2® Gillinov-Cosgrove™ LAA Exclusion System PRO235 A000965 2026-04-28 10840143913495 AtriClip PRO2® Gillinov-Cosgrove™ LAA Exclusion System PRO240 A000966 2026-04-28 10840143913501 AtriClip PRO2® Gillinov-Cosgrove™ LAA Exclusion System PRO245 A000967 2026-04-28 10840143913518 AtriClip PRO2® Gillinov-Cosgrove™ LAA Exclusion System PRO250 A000968 2026-04-28 10840143913525 AtriClip PROV® LAA Exclusion System PROV35 A000971-4 2026-04-28
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