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Device Explorer · FDA GUDID · GMDN 44784

Intermittent venous compression system pump

An electrically-powered device 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 with the necessary pressure to promote venous blood flow. This

US‑registered devices157in commercial distribution
Companies11labelers on GUDID
Single‑use24%of device records
Sterile0%labelled sterile
Prescription86%Rx‑only share
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Share of device records

Tactile Systems Technology, Inc.8957%
Sun Scientific, Inc.3321%
Microtek Medical Llc138%
Cavalier Alp, Llc53%
Compression Therapy Concepts, Inc.53%
Manamed, Inc.43%
Medline Industries, Inc.43%
Zimmer Orthopaedic Surgical Products, Inc.11%

Top labelers

CompanyDevicesShare
Tactile Systems Technology, Inc.8957%
Sun Scientific, Inc.3321%
Microtek Medical Llc138%
Cavalier Alp, Llc53%
Compression Therapy Concepts, Inc.53%
Manamed, Inc.43%
Medline Industries, Inc.43%
Zimmer Orthopaedic Surgical Products, Inc.11%
Currie Medical Inc.11%
Bio Compression Systems, Inc11%
Medi Manufacturing, Inc.11%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

VasoPress® DVT PumpALP® 900ALP®VasQcareAeroDVx™ Arm LargeAeroDVx™, Arm MediumAeroDVx™, Arm SmallAeroDVx™ Extra Large Flex BilateralAeroDVx™ Large Flex BilateralAeroDVx™, Medium Flex BilateralAeroDVx™, Small Flex BilateralAeroDVx™, Extra Large Flex UnilateralAeroDVx™, Large Flex UnilateralAeroDVx™, Medium Flex UnilateralAeroDVx™, Small Flex UnilateralAeroDVx ™

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

FDA product codes

CodeNameDevices
JOWSleeve, Limb, Compressible142
PPSSleeve, Head And Neck, Compressible75
JOWSLEEVE, LIMB, COMPRESSIBLE32
IRPMassager, Powered Inflatable Tube2

GMDN & GCC registration

  • GMDN code 44784 · non‑implantable
  • Single‑use 24% · sterile 0% · Rx‑only 86% · OTC 3%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Feet) · 6

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

No closely related category with 50+ devices.

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

157 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Intermittent venous compression system pump", from 11 companies. The largest labeler is Tactile Systems Technology, Inc. with 57% of records.

Which FDA product codes apply?

JOW (Sleeve, Limb, Compressible), PPS (Sleeve, Head And Neck, Compressible), JOW (SLEEVE, LIMB, COMPRESSIBLE), IRP (Massager, Powered Inflatable Tube)

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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