A mains electricity (AC-powered), external device designed for the application of rhythmic compression to the chest in the region of the heart to provide blood flow during treatment of cardiac arrest [cardiopulmonary resuscitation (CPR)]. The device may consis
| Company | Devices | Share |
|---|---|---|
| Zoll Circulation, Inc. | 209 | 92% |
| Defibtech, L.L.C. | 13 | 6% |
| Jolife Ab | 4 | 2% |
| Physio-Control, Inc. | 2 | 1% |
Company = labeler of record on GUDID. 4 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 |
|---|---|---|
| DRM | Compressor, Cardiac, External | 222 |
| DRM | Compressor, cardiac, external | 5 |
| DRM | COMPRESSOR, CARDIAC, EXTERNAL | 2 |
Use these as the dimensions to specify in a tender line.
228 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cardiac resuscitator, line-powered", from 4 companies. The largest labeler is Zoll Circulation, Inc. with 92% of records.
DRM (Compressor, Cardiac, External), DRM (Compressor, cardiac, external), DRM (COMPRESSOR, CARDIAC, EXTERNAL)
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.