FDA UDI In Commercial Distribution 🇺🇸 United States

Isolator Surgical Ablation System

DI: 10840143901980 · Model: MAX1 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
4
Pkg Device Count
1

Basic Information

Brand Name
Isolator Surgical Ablation System
Primary DI
10840143901980
Version / Model
MAX1
Catalog Number
A000163
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
2
Public Version Date
2022-06-10
Public Version Status
Update
Public Device Record Key
39eb831a-f519-41af-80c5-8f4f375486cd

Device Description

Isolator Transpolar Pen

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

GMDN Terms

Code Name
60784 Cardiac radio-frequency ablation system generator

Identifiers

Type ID
Package 30840143901984
Primary 10840143901980
Package 50840143900042
Previous 00818354010343

Customer Contacts

Phone
866-349-2342