FDA UDI In Commercial Distribution 🇺🇸 United States

Fusion Ablation System

DI: 00818354012811 · Model: 001-700-002 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Fusion Ablation System
Primary DI
00818354012811
Version / Model
001-700-002
Company Name
ATRICURE, INC.
Labeler DUNS
006133784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-24
Public Version
5
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
77fc65e6-87f5-42b8-8689-21a165a7bd4e

Device Description

Fusion 50 Ablation System

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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OCL Surgical Device, For Cutting, Coagulation, And/Or Ablation Of Tissue, Including Cardiac Tissue

GMDN Terms

Code Name
44776 Electrosurgical system

Identifiers

Type ID
Primary 00818354012811

Customer Contacts

Phone
866-349-2342

Device Sizes

Type Value Unit Text
Length 50 Millimeter

Storage Conditions

Type
Special Storage Condition, Specify
Special Conditions
Store in a cool, dry place