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Device Explorer · FDA GUDID · GMDN 47367

Emergency airway clearance suction system, pneumatic

A portable assembly of devices, which includes a non-surgical invasive component, intended to aspirate unwanted materials (e.g., fluids, secretions) from the airway typically during patient transport or an emergency situation (e.g., placed on a crash cart), by

US‑registered devices95in commercial distribution
Companies4labelers on GUDID
Single‑use2%of device records
Sterile0%labelled sterile
Prescription3%Rx‑only share
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Share of device records

W. T. Farley, Inc.9196%
O-Two Medical Technologies Inc22%
Gmmi Sdn. Bhd.11%
Allied Medical, Llc11%

Top labelers

CompanyDevicesShare
W. T. Farley, Inc.9196%
O-Two Medical Technologies Inc22%
Gmmi Sdn. Bhd.11%
Allied Medical, Llc11%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

STATVAC II Oxygen powered AspiratorSüpeVac – Portable Single Use Hand-Held Suction Du-O-VacLSP

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

FDA product codes

CodeNameDevices
GCXAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED91
BTAPump, Portable, Aspiration (Manual Or Powered)3
KDQBottle, Collection, Vacuum1

GMDN & GCC registration

  • GMDN code 47367 · non‑implantable
  • Single‑use 2% · sterile 0% · Rx‑only 3% · 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

Pressure (Pound per Square Inch) · 91Total Volume (Fluid Ounce) · 2

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

How many emergency airway clearance suction system, pneumatic products are registered in the US?

95 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Emergency airway clearance suction system, pneumatic", from 4 companies. The largest labeler is W. T. Farley, Inc. with 96% of records.

Which FDA product codes apply?

GCX (APPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED), BTA (Pump, Portable, Aspiration (Manual Or Powered)), KDQ (Bottle, Collection, Vacuum)

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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