Device Explorer · FDA GUDID · GMDN 15270

Sump drain

A sterile, tube-like device that has a double lumen which is designed to establish a channel for the removal of fluids from a cavity by allowing air to enter the cavity through the smaller lumen which displaces fluid into the larger lumen. This is a single-use

US‑registered devices106in commercial distribution
Companies6labelers on GUDID
Single‑use98%of device records
Sterile90%labelled sterile
Prescription86%Rx‑only share
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Share of device records

Axiom Medical, Incorporated5855%
Cardinal Health 200, Llc1918%
Armm Inc.1110%
Fortune Medical Instrument Corp.98%
Cardinal Health, Inc.77%
Surgix Medical Llc22%

Top labelers

CompanyDevicesShare
Axiom Medical, Incorporated5855%
Cardinal Health 200, Llc1918%
Armm Inc.1110%
Fortune Medical Instrument Corp.98%
Cardinal Health, Inc.77%
Surgix Medical Llc22%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

ArgyleGen2Salem SumpSilicone Sump Drain TubeKangarooMedDrainAxiom®Axiom® CWV Sump Atraum™ With ClotStop®Axiom® Interpleural Anesthesia Atraum™ With ClotAxiom® Interpleural AnesthesiaAxiom® Dual-SumpAxiom® Dual-Sump Atraum™ With ClotStop®Axiom® Uni-Sump Atraum™ With ClotStop®Axiom® Uni-SumpAxiom® Mills Sump Atraum™ With ClotStop®Axiom® Mills Sump

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

FDA product codes

CodeNameDevices
GBSCatheter, Ventricular, General & Plastic Surgery27
FEGTube, Double Lumen For Intestinal Decompression And/Or Intub25
FEGTUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUB14
GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY11
KNTTubes, gastrointestinal (and accessories)10
GBNCatheter, Pediatric, General & Plastic Surgery10

GMDN & GCC registration

  • GMDN code 15270 · non‑implantable
  • Single‑use 98% · sterile 90% · Rx‑only 86% · OTC 6%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Length (Inch) · 64Lumen/Inner Diameter (Millimeter) · 38Catheter Gauge (French) · 32Lumen/Inner Diameter (Inch) · 6Angle (degree) · 2Length (Centimeter) · 1

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

No closely related category with 50+ devices.

How many sump drain products are registered in the US?

106 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Sump drain", from 6 companies. The largest labeler is Axiom Medical, Incorporated with 55% of records.

Which FDA product codes apply?

GBS (Catheter, Ventricular, General & Plastic Surgery), FEG (Tube, Double Lumen For Intestinal Decompression And/Or Intub), FEG (TUBE, DOUBLE LUMEN FOR INTESTINAL DECOMPRESSION AND/OR INTUB), GEA (CANNULA, SURGICAL, GENERAL & PLASTIC SURGERY)

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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