A flexible wire with an electrode, insulated with non-conductive material except at its ends, that serves as an electrical conductor between the heart and an external temporary pacing/defibrillation device used to treat postoperative cardiac arrhythmias/cardia
| Company | Devices | Share |
|---|---|---|
| A & E Medical Corporation | 185 | 78% |
| Oscor Inc. | 27 | 11% |
| Ethicon, Llc | 12 | 5% |
| Covidien Lp | 9 | 4% |
| Medtronic, Inc. | 5 | 2% |
Company = labeler of record on GUDID. 5 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 |
|---|---|---|
| LDF | ELECTRODE, PACEMAKER, TEMPORARY | 158 |
| LDF | Electrode, Pacemaker, Temporary | 87 |
Use these as the dimensions to specify in a tender line.
No closely related category with 50+ devices.
238 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Transthoracic pacing lead", from 5 companies. The largest labeler is A & E Medical Corporation with 78% of records.
LDF (ELECTRODE, PACEMAKER, TEMPORARY), LDF (Electrode, Pacemaker, Temporary)
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.