FDA UDI
In Commercial Distribution
🇺🇸 United States
HeartLight
DI: 00859373007464
·
Model: 18-4957
·
CARDIOFOCUS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1
Basic Information
- Brand Name
- HeartLight
- Primary DI
- 00859373007464
- Version / Model
- 18-4957
- Catalog Number
- 18-4957
- 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
- b0ba7805-b7b9-4b4e-bd55-5dd40480c1d9
Device Description
HeartLight X3 Console, EU
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 | Medical Specialty | Regulation # | Device Class |
|---|---|---|---|---|
| OAE | Catheter, percutaneous, cardiac ablation, for treatment of atrial fibrillation | Unknown | 3 |
GMDN Terms
| Code | Name | Definition | Implantable | Status |
|---|---|---|---|---|
| 61969 | Cardiac ablation solid-state laser system | A mains electricity (AC-powered) device assembly in which input energy (e.g., flashlamp, diode laser) is used to excite a doped glass/crystal medium to emit a high-power laser beam intended for endocardial ablation procedures for the treatment of atrial fibrillation; the therapeutic laser does not include frequency-doubling technology. It includes a laser generator with controls and monitor. It is intended to function with a laser beam-guide catheter (typically introduced to the pulmonary vein via transseptal access) and a flexible video angioscope for visualization during the procedure; the catheter and angioscope may be included. | No | Active |
Identifiers
| Type | ID | Issuing Agency | Package Type | Qty per Pkg | Pkg Status | Pkg Discontinue Date |
|---|---|---|---|---|---|---|
| Primary | 00859373007464 | GS1 |
Customer Contacts
- Phone
- +1(844)527-3723
- [email protected]
Premarket Submissions
| Submission Number | Supplement Number |
|---|---|
| P150026 | 008 |
Storage Conditions
- Type
- Storage Environment Temperature
- Temperature Range
- -25 – 55 Degrees Celsius