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Device Explorer · FDA GUDID · GMDN 10969

Intermittent venous compression system

A system used for the noninvasive treatment and prevention of venous disorders and sequelae such as oedema, deep vein thrombosis (DVT) and pulmonary embolism (PE). It functions by intermittently applying pressure to a patient's arms or legs to promote venous b

US‑registered devices403in commercial distribution
Companies28labelers on GUDID
Single‑use13%of device records
Sterile0%labelled sterile
Prescription61%Rx‑only share
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Share of device records

Daesung Maref Co.,Ltd.10727%
Normatec Industries Lp10025%
Djo, Llc307%
Rapid Reboot Recovery Products Llc215%
Arjohuntleigh Ab195%
Medhealth Medical Limited174%
Precision Medical Products, Inc.164%
Medline Industries, Inc.123%

Top labelers

CompanyDevicesShare
Daesung Maref Co.,Ltd.10727%
Normatec Industries Lp10025%
Djo, Llc307%
Rapid Reboot Recovery Products Llc215%
Arjohuntleigh Ab195%
Medhealth Medical Limited174%
Precision Medical Products, Inc.164%
Medline Industries, Inc.123%
Guangzhou Pinzhi Medical Technology Co., Ltd113%
Caremed Supply Inc.113%
Manamed, Inc.113%
Compedica Limited102%

Company = labeler of record on GUDID. 28 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Air wave pressure circulation massagerCompression Therapy DeviceMedHealthReefanPressure Therapy SystemLegacy IPCPulseFlow DF™FLOWTRON ACS900Prius Healthcare USAAIRCASTEMPIArtAssistAIROSGo Green Barrier SleeveM-31 Reusable Universal Calf GarmentPlasmaFlow X

Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.

FDA product codes

CodeNameDevices
IRPMassager, Powered Inflatable Tube260
JOWSleeve, Limb, Compressible205
JOWSLEEVE, LIMB, COMPRESSIBLE95
ISAMassager, Therapeutic, Electric11
ILOPack, Hot Or Cold, Water Circulating2
FDElaparoscopy kit1

GMDN & GCC registration

  • GMDN code 10969 · non‑implantable
  • Single‑use 13% · sterile 0% · Rx‑only 61% · OTC 38%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Millimeter) · 6

Use these as the dimensions to specify in a tender line.

How many intermittent venous compression system products are registered in the US?

403 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intermittent venous compression system", from 28 companies. The largest labeler is Daesung Maref Co.,Ltd. with 27% of records.

Which FDA product codes apply?

IRP (Massager, Powered Inflatable Tube), JOW (Sleeve, Limb, Compressible), JOW (SLEEVE, LIMB, COMPRESSIBLE), ISA (Massager, Therapeutic, Electric)

Is this the same as UAE/GCC registration?

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.

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