An electrical conductor intended to be used in pairs to transmit a controlled electrical shock from an external defibrillator to a post-pubescent patient to defibrillate the heart (restore normal rhythm) or slow a rapid heart rate. It typically consists of a c
| Company | Devices | Share |
|---|---|---|
| Cardio-Medical Products, Inc. | 28 | 28% |
| Physio-Control, Inc. | 11 | 11% |
| Graphic Controls Acquisition Corp | 11 | 11% |
| Fiab Spa | 11 | 11% |
| Zoll Medical Corporation | 8 | 8% |
| Vive Health Llc | 7 | 7% |
| Defibtech, L.L.C. | 7 | 7% |
| Philips Medical Systems Hsg | 5 | 5% |
| Philips Electronics North America Corporation | 4 | 4% |
| Cardiac Science Corporation | 4 | 4% |
| Resource Optimization & Innovation, L.L.C. | 3 | 3% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| MKJ | Automated External Defibrillators (Non-Wearable) | 39 |
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) | 39 |
| MKJ | Automated external defibrillators (non-wearable) | 19 |
| GXY | Electrode, Cutaneous | 7 |
| MLN | Electrode, Electrocardiograph, Multi-Function | 4 |
| NSA | Over-The-Counter Automated External Defibrillator | 1 |
Use these as the dimensions to specify in a tender line.
99 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "External defibrillation electrode, adult, single-use", from 11 companies. The largest labeler is Cardio-Medical Products, Inc. with 28% of records.
MKJ (Automated External Defibrillators (Non-Wearable)), LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)), MKJ (Automated external defibrillators (non-wearable)), GXY (Electrode, Cutaneous)
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.