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Device Explorer · FDA GUDID · GMDN 10217

Surgical suction system

An assembly of devices designed to evacuate large volumes of gas, liquid, tissue and/or other debris from a surgical site by means of suction during surgical procedures. It generally consists of a mains electricity (AC-powered) suction pump, a regulator and ga

US‑registered devices103in commercial distribution
Companies5labelers on GUDID
Single‑use4%of device records
Sterile2%labelled sterile
Prescription92%Rx‑only share
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Share of device records

Karl Storz Gmbh & Co. Kg8784%
Pentax Of America, Inc.55%
Rico Suction Labs Inc55%
Medical Device Resource Corporation33%
Avante33%

Top labelers

CompanyDevicesShare
Karl Storz Gmbh & Co. Kg8784%
Pentax Of America, Inc.55%
Rico Suction Labs Inc55%
Medical Device Resource Corporation33%
Avante33%

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

Brand names on the register (sample)

N/AVARIOn.a.TAKE-APARTENDOMATRico Suction Labs, Inc.MD ResourceDM-660DM-530

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

FDA product codes

CodeNameDevices
EOXESOPHAGOSCOPE (FLEXIBLE OR RIGID)40
BTAPump, Portable, Aspiration (Manual Or Powered)10
GWGENDOSCOPE, NEUROLOGICAL10
GCJLaparoscope, general & plastic surgery6
EOXEsophagoscope (flexible or rigid)6
GCXAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED5

GMDN & GCC registration

  • GMDN code 10217 · non‑implantable
  • Single‑use 4% · sterile 2% · Rx‑only 92% · 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 surgical suction system products are registered in the US?

103 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical suction system", from 5 companies. The largest labeler is Karl Storz Gmbh & Co. Kg with 84% of records.

Which FDA product codes apply?

EOX (ESOPHAGOSCOPE (FLEXIBLE OR RIGID)), BTA (Pump, Portable, Aspiration (Manual Or Powered)), GWG (ENDOSCOPE, NEUROLOGICAL), GCJ (Laparoscope, 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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