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Device Explorer · FDA GUDID · GMDN 47998

Surgical fluid/smoke waste management system

An assembly of devices designed to collect and dispose of both surgical fluid waste and plume smoke generated by surgical procedures involving electrosurgical diathermy, electrocautery, or a laser. It typically consists of a mains electricity (AC-powered) mobi

US‑registered devices50in commercial distribution
Companies3labelers on GUDID
Single‑use38%of device records
Sterile18%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Stryker Corporation3570%
Alesi Surgical Limited1224%
Medline Industries, Inc.36%

Top labelers

CompanyDevicesShare
Stryker Corporation3570%
Alesi Surgical Limited1224%
Medline Industries, Inc.36%

Company = labeler of record on GUDID. 3 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

NeptuneNANeptune 2UltravisionTMUltravsionTMNakao QuicktrapMEDLINE

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

FDA product codes

CodeNameDevices
JCXAPPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED27
FYDAPPARATUS, EXHAUST, SURGICAL24
PQMSurgical Smoke Precipitator12
GEIElectrosurgical, cutting & coagulation & accessories3
GCXAPPARATUS, SUCTION, OPERATING-ROOM, WALL VACUUM POWERED1
BYZTRAP, STERILE SPECIMEN1

GMDN & GCC registration

  • GMDN code 47998 · non‑implantable
  • Single‑use 38% · sterile 18% · Rx‑only 100% · 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

Length (Meter) · 4Length (Feet) · 2

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

How many surgical fluid/smoke waste management system products are registered in the US?

50 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Surgical fluid/smoke waste management system", from 3 companies. The largest labeler is Stryker Corporation with 70% of records.

Which FDA product codes apply?

JCX (APPARATUS, SUCTION, WARD USE, PORTABLE, AC-POWERED), FYD (APPARATUS, EXHAUST, SURGICAL), PQM (Surgical Smoke Precipitator), GEI (Electrosurgical, cutting & coagulation & accessories)

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.

How do I get quotes?

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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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