FDA UDI In Commercial Distribution 🇺🇸 United States

HeartLight

DI: 00859373007440 · Model: 18-4952 · CARDIOFOCUS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
HeartLight
Primary DI
00859373007440
Version / Model
18-4952
Catalog Number
18-4952
Company Name
CARDIOFOCUS, INC.
Labeler DUNS
068966261
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-05-19
Public Version
1
Public Version Date
2020-05-27
Public Version Status
New
Public Device Record Key
4252a5d3-76b8-486d-a030-2a677d1299c1

Device Description

HeartLight X3 Console, US

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
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
OAE Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation

GMDN Terms

Code Name
61969 Cardiac ablation solid-state laser system

Identifiers

Type ID
Primary 00859373007440

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P150026 008

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-25 – 55 Degrees Celsius