An electrically-powered, noninvasive device designed to be worn by a patient during daily activities for 24-hour recording of the electrocardiographic signals of the heart, for the diagnosis of cardiac disorders (e.g., arrhythmias). The recorded measurements c
| Company | Devices | Share |
|---|---|---|
| Welch Allyn, Inc. | 60 | 17% |
| Norav Medical Ltd. | 56 | 16% |
| Global Instrumentation, Llc | 43 | 13% |
| Braemar Manufacturing, Llc | 33 | 10% |
| Vasomedical, Inc. | 31 | 9% |
| Getemed Medizin- Und Informationstechnik Ag | 19 | 6% |
| Spacelabs Healthcare (Washington), Inc | 14 | 4% |
| Datrix Llc | 10 | 3% |
| Microport Crm Srl | 9 | 3% |
| Mortara Instrument, Inc. | 7 | 2% |
| Icentia Inc. | 6 | 2% |
| Dm Systems (Beijing) Co., Ltd. | 5 | 1% |
Company = labeler of record on GUDID. 34 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 |
|---|---|---|
| MWJ | Electrocardiograph, ambulatory (without analysis) | 106 |
| MWJ | Electrocardiograph, Ambulatory (Without Analysis) | 94 |
| MWJ | Electrocardiograph,Ambulatory(Without Analysis) | 54 |
| DSH | Recorder, Magnetic Tape, Medical | 52 |
| DSH | RECORDER, MAGNETIC TAPE, MEDICAL | 50 |
| MLO | Electrocardiograph, Ambulatory, With Analysis Algorithm | 37 |
Use these as the dimensions to specify in a tender line.
343 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Electrocardiographic ambulatory recorder", from 34 companies. The largest labeler is Welch Allyn, Inc. with 17% of records.
MWJ (Electrocardiograph, ambulatory (without analysis)), MWJ (Electrocardiograph, Ambulatory (Without Analysis)), MWJ (Electrocardiograph,Ambulatory(Without Analysis)), DSH (Recorder, Magnetic Tape, Medical)
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.