FDA UDI In Commercial Distribution 🇺🇸 United States

Synergy™ Ablation System

DI: 10840143902192 · Model: OSL2 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Synergy™ Ablation System
Primary DI
10840143902192
Version / Model
OSL2
Catalog Number
A000432
Company Name
ATRICURE, INC.
Labeler DUNS
006133784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-01-08
Public Version
4
Public Version Date
2023-05-29
Public Version Status
Update
Public Device Record Key
9d0036d8-73f5-4e4f-9bbe-47ae51e0c427

Device Description

Isolator Synergy™ Surgical Ablation System Open, Short Jaw, Left Curve

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
No
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
OCM Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation

GMDN Terms

Code Name
60784 Cardiac radio-frequency ablation system generator

Identifiers

Type ID
Package 30840143902318
Primary 10840143902192
Package 50840143902244
Previous 00818354010558

Customer Contacts

Phone
866-349-2342

Premarket Submissions

Submission Number Supplement Number
P100046 003
P100046 004
P100046 005
P100046 006
P100046 007
P100046 008
P100046 009
P100046 010
P100046 011
P100046 012
P100046 013
P100046 016