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Device Explorer · FDA GUDID · GMDN 61809

Single-chamber venous compression system garment, reprocessed

A non-sterile, inflatable device in the form of a stocking, sleeve, or suit intended to be applied to the limbs externally to promote venous blood flow. As part of a compression system, the device applies pressure to the extremities through the intermittent in

US‑registered devices104in commercial distribution
Companies5labelers on GUDID
Single‑use89%of device records
Sterile0%labelled sterile
Prescription90%Rx‑only share
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Share of device records

Medline Industries, Inc.5048%
Stryker Sustainability Solutions, Inc.4038%
Cavalier Alp, Llc1010%
Cardinal Health 200, Llc33%
Allied Medical, Llc11%

Top labelers

CompanyDevicesShare
Medline Industries, Inc.5048%
Stryker Sustainability Solutions, Inc.4038%
Cavalier Alp, Llc1010%
Cardinal Health 200, Llc33%
Allied Medical, Llc11%

Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

n/aN/ARE-CUR PVA/ALP®RE-CUR ALP®Allied Medical LLCKendallMEDLINEMedline ReNewalMEDLINE RENEWALCARDINAL HEALTH

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, COMPRESSIBLE125
JOWSleeve, Limb, Compressible32
KPJChamber, Oxygen, Topical, Extremity1

GMDN & GCC registration

  • GMDN code 61809 · non‑implantable
  • Single‑use 89% · sterile 0% · Rx‑only 90% · OTC 0%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Circumference (Inch) · 16

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

How many single-chamber venous compression system garment, reprocessed products are registered in the US?

104 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Single-chamber venous compression system garment, reprocessed", from 5 companies. The largest labeler is Medline Industries, Inc. with 48% of records.

Which FDA product codes apply?

JOW (SLEEVE, LIMB, COMPRESSIBLE), JOW (Sleeve, Limb, Compressible), KPJ (Chamber, Oxygen, Topical, Extremity)

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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