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Device Explorer · FDA GUDID · GMDN 36778

General-purpose suction system, vacuum

An assembly of devices designed to evacuate fluid, tissue, gas, or foreign materials from a body cavity or lumen by means of suction. It is connected via dedicated vacuum tubing to the vacuum terminal unit (wall outlet) of a vacuum pipeline system and powered

US‑registered devices106in commercial distribution
Companies4labelers on GUDID
Single‑use46%of device records
Sterile0%labelled sterile
Prescription61%Rx‑only share
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Share of device records

Amsino International, Inc.7369%
Amico Patient Care Corporation3129%
Smith & Nephew, Inc.11%
Skyline Medical Inc.11%

Top labelers

CompanyDevicesShare
Amsino International, Inc.7369%
Amico Patient Care Corporation3129%
Smith & Nephew, Inc.11%
Skyline Medical Inc.11%

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

Brand names on the register (sample)

Amico Patient Care CorporationBIRMINGHAMHIPRESURFACING(BHR)RECEPTAL™ WALL CHANNEL BRACKET FOR CANISTER SUPPRECEPTAL™ CANISTER SUPPORT FOR 3000MLRECEPTAL™ CANISTER SUPPORT FOR 1000ML, 1500ML ANREGULATOR MOUNT CANISTER EXTENDERCANISTER SUPPORT BRACKET TO ATTACH CANISTER DIREBRACKET CLAMPADJUSTABLE-HEIGHT, SMALL HEAD, STAINLESS STEEL FADJUSTABLE-HEIGHT, LARGE HEAD, STAINLESS STEEL FEZE-VAC® CANISTER RING SUPPORTRECEPTAL™ IN-LINE QUAD FLOOR STAND, STAINLESS STRECEPTAL™ TANDEM FLOOR STAND, STAINLESS STEEL WIRECEPTAL™ SINGLE FLOOR STANDRECEPTAL™ TANDEM LONG CANISTER SUPPORT USE WITH RECEPTAL™ SINGLE LONG CANISTER SUPPORT WITH MOUN

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 Powered74
KDPRegulator, Vacuum31
NXTProsthesis, hip, semi-constrained, metal/metal, resurfacing1

GMDN & GCC registration

  • GMDN code 36778 · non‑implantable
  • Single‑use 46% · sterile 0% · Rx‑only 61% · 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

Height (Inch) · 1

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

How many general-purpose suction system, vacuum 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 "General-purpose suction system, vacuum", from 4 companies. The largest labeler is Amsino International, Inc. with 69% of records.

Which FDA product codes apply?

GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered), KDP (Regulator, Vacuum), NXT (Prosthesis, hip, semi-constrained, metal/metal, resurfacing)

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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