A sterile, flexible, steerable catheter intended to be used as part of a radio-frequency cardiac ablation system to apply radio-frequency alternating current to ablate areas of the endocardium of a beating heart in the treatment of cardiac arrhythmias; it is t
| Company | Devices | Share |
|---|---|---|
| Biosense Webster Inc | 213 | 49% |
| Boston Scientific Corporation | 85 | 19% |
| St. Jude Medical, Inc. | 42 | 10% |
| Medtronic, Inc. | 39 | 9% |
| Irvine Biomedical, Inc. | 36 | 8% |
| St. Jude Medical Cardiovascular Division | 21 | 5% |
| Osypka Gmbh | 1 | 0% |
Company = labeler of record on GUDID. 7 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| LPB | Cardiac ablation percutaneous catheter | 221 |
| OAD | catheter, percutaneous, cardiac ablation, for treatment of a | 194 |
| DRF | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING | 67 |
| OAE | Catheter, percutaneous, cardiac ablation, for treatment of a | 49 |
| QZI | Percutaneous Cardiac Ablation Catheter for Treatment of Atri | 5 |
| LPB | Cardiac Ablation Percutaneous Catheter | 1 |
Use these as the dimensions to specify in a tender line.
437 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiac radio-frequency ablation system catheter", from 7 companies. The largest labeler is Biosense Webster Inc with 49% of records.
LPB (Cardiac ablation percutaneous catheter), OAD (catheter, percutaneous, cardiac ablation, for treatment of a), DRF (CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING), OAE (Catheter, percutaneous, cardiac ablation, for treatment of a)
No. GUDID is the US register. For the UAE (MOHAP/DoH) and Saudi (SFDA/MDMA) a separate registration and a local authorised representative are required; Consulting Wallah can check the status and connect you with registered suppliers.
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Source: FDA AccessGUDID (AccessGUDID full release 2 Nov 2026); counts are device records in commercial distribution grouped by GMDN preferred term; companies are labelers of record. Information only — US listing is not a registration in the UAE or GCC; verify with the regulator. © Consulting Wallah — CC BY‑NC‑ND.