A noninvasive conductive material designed to facilitate electrical conduction between an external electrode (e.g., paddle-type defibrillator electrode) and the skin surface. It is available in various forms such as a thickened gel or polymer medium reinforced
| Company | Devices | Share |
|---|---|---|
| Tz Medical, Inc. | 31 | 19% |
| Heart Sync Inc | 27 | 16% |
| Resource Optimization & Innovation, L.L.C. | 21 | 13% |
| Medline Industries, Inc. | 20 | 12% |
| Graphic Controls Acquisition Corp | 15 | 9% |
| Bound Tree Medical, Llc | 13 | 8% |
| Cardinal Health 200, Llc | 10 | 6% |
| Drive Devilbiss Healthcare | 7 | 4% |
| Henry Schein, Inc. | 6 | 4% |
| Pacific West Medical, Inc. | 3 | 2% |
| Ace Surgical Supply Co., Inc. | 3 | 2% |
| Cardinal Health, Inc. | 3 | 2% |
Company = labeler of record on GUDID. 16 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 |
|---|---|---|
| LDD | Dc-Defibrillator, Low-Energy, (Including Paddles) | 61 |
| DRO | Pacemaker, Cardiac, External Transcutaneous (Non-Invasive) | 44 |
| MLN | Electrode, Electrodcardiograph, Multi-Function | 40 |
| MKJ | Automated External Defibrillators (Non-Wearable) | 25 |
| MKJ | Automated external defibrillators (non-wearable) | 24 |
| MLN | Electrode, electrocardiograph, multi-function | 18 |
Use these as the dimensions to specify in a tender line.
167 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electrode conductive skin pad, single-use", from 16 companies. The largest labeler is Tz Medical, Inc. with 19% of records.
LDD (Dc-Defibrillator, Low-Energy, (Including Paddles)), DRO (Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)), MLN (Electrode, Electrodcardiograph, Multi-Function), MKJ (Automated External Defibrillators (Non-Wearable))
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.