UDI device identifier
VARIPULSE™ Bi-Directional Catheter D141201
UDI device identifier 10846835025460 · Biosense Webster Inc
Key facts
| Primary DI | 10846835025460 |
|---|---|
| Brand name | VARIPULSE™ Bi-Directional Catheter |
| Version or model | D141201 |
| Catalog number | D141201 |
| Company | Biosense Webster Inc |
| DUNS number | 020163218 |
| Product code | QZI |
| GMDN term | Cardiac irreversible electroporation system catheter |
| Premarket submission | P240006 |
| Device class | Class III |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 11, 2024 |
| Version date | Sep 23, 2025 |
| Description | 8.5 FR VARIPULSE™ Bi-Directional Catheter |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: