FDA UDI In Commercial Distribution 🇺🇸 United States

EPi-Sense Guided Coagulation System with VisiTrax

DI: 10840143904554 · Model: CDK-1413 · ATRICURE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
3
Pkg Device Count
1

Basic Information

Brand Name
EPi-Sense Guided Coagulation System with VisiTrax
Primary DI
10840143904554
Version / Model
CDK-1413
Catalog Number
CDK-1413-3
Company Name
ATRICURE, INC.
Labeler DUNS
006133784
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-05-24
Public Version
5
Public Version Date
2023-05-29
Public Version Status
Update
Public Device Record Key
1239ebde-ff20-4167-a932-e28f30532c9b

Device Description

3 cm Guided Coagulation System Kit

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
Primary 10840143904554
Package 30840143903827
Package 50840143903364

Customer Contacts

Phone
866-349-2342

Premarket Submissions

Submission Number Supplement Number
K120857 000
K142084 000
P200002 000
P200002 004
P200002 005

Device Sizes

Type Value Unit Text
Length 3 Centimeter