An electrically-powered device intended to be used for the noninvasive treatment and prevention of venous disorders/sequelae. As part of a compression system, the pump provides the connected stocking/sleeve/suit applied to the extremities with the necessary pr
| Company | Devices | Share |
|---|---|---|
| Daesung Maref Co.,Ltd. | 66 | 23% |
| Maxstar Industrial Co.,Ltd. | 42 | 15% |
| Bio Compression Systems, Inc | 40 | 14% |
| Wright Therapy Products, Inc. | 36 | 13% |
| Medical Compression System (D.B.N.) Ltd. | 15 | 5% |
| Cardinal Health, Inc. | 13 | 5% |
| Mego Afek Agricultural Cooperative Society Ltd | 12 | 4% |
| Cardinal Health 200, Llc | 11 | 4% |
| Zimmer Orthopaedic Surgical Products, Inc. | 9 | 3% |
| Compression Solutions, Llc | 7 | 2% |
| Airos Medical Inc | 7 | 2% |
| Wonjin Mulsan Co.Ltd | 6 | 2% |
Company = labeler of record on GUDID. 22 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 |
|---|---|---|
| JOW | SLEEVE, LIMB, COMPRESSIBLE | 125 |
| IRP | Massager, Powered Inflatable Tube | 108 |
| JOW | Sleeve, Limb, Compressible | 82 |
| IRO | Vibrator, Therapeutic | 3 |
| ILY | Lamp, Infrared, Therapeutic Heating | 3 |
| LXB | Hearing aid, bone conduction | 3 |
Use these as the dimensions to specify in a tender line.
285 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Sequential venous compression system inflator", from 22 companies. The largest labeler is Daesung Maref Co.,Ltd. with 23% of records.
JOW (SLEEVE, LIMB, COMPRESSIBLE), IRP (Massager, Powered Inflatable Tube), JOW (Sleeve, Limb, Compressible), IRO (Vibrator, Therapeutic)
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.