Primary Device ID | 30840143901625 |
NIH Device Record Key | b63f7220-26d4-4f52-ac04-4a6e22b4fe3e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Synergy™ Ablation System |
Version Model Number | GPT300 |
Catalog Number | A000437 |
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 Issuing Agency | Device ID |
---|---|
GS1 | 00818354010718 [Previous] |
GS1 | 10840143900020 [Primary] |
GS1 | 30840143901625 [Package] Contains: 10840143900020 Package: box [1 Units] In Commercial Distribution |
GS1 | 50840143903074 [Package] Package: case [18 Units] In Commercial Distribution |
FZX | Guide, Surgical, Instrument |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-01-18 |
Device Publish Date | 2021-01-08 |
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) |