FDA UDI In Commercial Distribution 🇺🇸 United States

Cardiodrive System

DI: M588001004115110 · Model: II · STEREOTAXIS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Cardiodrive System
Primary DI
M588001004115110
Version / Model
II
Catalog Number
001-004115-11
Company Name
STEREOTAXIS, INC.
Labeler DUNS
024942265
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-06
Public Version
1
Public Version Date
2022-06-14
Public Version Status
New
Public Device Record Key
0a81a8c3-134e-4c1e-bc49-e7f3de9899a7

Device Description

The Stereotaxis Cardiodrive is intended for automatically advancing and retracting only compatible magnetic electrophysiology (EP) mapping and ablation catheters inside the patient's heart when used in conjunction with a Stereotaxis Magnetic Navigation System (MNS). It is not intended to advance the EP mapping and ablation catheters through the coronary vasculature nor the coronary sinus.

Device Characteristics

Single Use
No
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
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
DQX Wire, Guide, Catheter

GMDN Terms

Code Name
38723 Robotic surgical navigation system

Identifiers

Type ID
Primary M588001004115110

Customer Contacts

Phone
13146786100

Premarket Submissions

Submission Number Supplement Number
K071029 000