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Device Explorer · FDA GUDID · GMDN 44809

Vacuum suction regulator/regulation set, general-purpose

A noninvasive device/collection of noninvasive devices designed to connect to the terminal unit (wall outlet) of a vacuum pipeline system to control the degree of negative pressure during the evacuation of fluids, mucus, or solids during a range of clinical ap

US‑registered devices1,612in commercial distribution
Companies15labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription91%Rx‑only share
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Share of device records

Allied Medical, Llc83652%
Medline Industries, Inc.42126%
Ohio Medical, Llc1509%
Precision Medical, Inc.835%
Boehringer Laboratories, Llc413%
Hersill Sl241%
Penlon Ltd201%
Tenacore Holdings, Inc.91%

Top labelers

CompanyDevicesShare
Allied Medical, Llc83652%
Medline Industries, Inc.42126%
Ohio Medical, Llc1509%
Precision Medical, Inc.835%
Boehringer Laboratories, Llc413%
Hersill Sl241%
Penlon Ltd201%
Tenacore Holdings, Inc.91%
Gentec(Shanghai)Corporation70%
Drägerwerk Ag & Co. Kgaa70%
Gce, S.R.O.60%
Smith & Nephew, Inc.40%

Company = labeler of record on GUDID. 15 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Amico Patient Care CorporationGENTEC®Suction Regulator, Stainless Steel with ImprovedPenlonSC760 MRI Suction Controller 2m hoseSC760 MRI Suction Controller 4m hoseVarioVac P rail DissVarioVac B/OR rail DissVarioVac MRI B/OR railVarioVac MRI P railSilicone hose 6x2,5 2mVacumaspirator Diss CanadaNozzle water vacuum gaugeDYOVACN/AVario AC

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 Powered810
KDPRegulator, Vacuum441
KDPREGULATOR, VACUUM420
NBHACCESSORIES,ARTHROSCOPIC5
GAZTubing, Noninvasive4
GCXAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED2

GMDN & GCC registration

  • GMDN code 44809 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 91% · 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

No structured size data on the register.

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

How many vacuum suction regulator/regulation set, general-purpose products are registered in the US?

1,612 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Vacuum suction regulator/regulation set, general-purpose", from 15 companies. The largest labeler is Allied Medical, Llc with 52% of records.

Which FDA product codes apply?

GCX (Apparatus, Suction, Operating-Room, Wall Vacuum Powered), KDP (Regulator, Vacuum), KDP (REGULATOR, VACUUM), NBH (ACCESSORIES,ARTHROSCOPIC)

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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