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Device Explorer · FDA GUDID · GMDN 47559

Water jet knife system handpiece, single-use

A sterile, hand-operated device that is a component of a water jet knife system and designed to direct a concentrated stream of high-pressure water (typically sterile saline) to a surgical site to cut/dissect tissue. This handpiece is connected to a generator

US‑registered devices57in commercial distribution
Companies4labelers on GUDID
Single‑use93%of device records
Sterile98%labelled sterile
Prescription51%Rx‑only share
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Share of device records

Hydrocision, Inc.3256%
Smith & Nephew Medical Limited916%
Erbe Elektromedizin Gmbh916%
Procept Biorobotics Corporation712%

Top labelers

CompanyDevicesShare
Hydrocision, Inc.3256%
Smith & Nephew Medical Limited916%
Erbe Elektromedizin Gmbh916%
Procept Biorobotics Corporation712%

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

Brand names on the register (sample)

VERSAJET III PRECISION Hydrosurgery System Hand ERBESpineJet® PerResector-China VersionAllograft-ALTAllograftQuickKart Procedure CartSpineJet®CannulaTrephineKnobTenJet®AquaBeam HandpieceHYDROS HandpieceVersajet

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

FDA product codes

CodeNameDevices
HRXArthroscope31
FQHLavage, Jet9
FQHLAVAGE, JET9
PZPFluid jet removal system6
PZPFluid Jet Removal System1

GMDN & GCC registration

  • GMDN code 47559 · non‑implantable
  • Single‑use 93% · sterile 98% · Rx‑only 51% · 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 (Millimeter) · 8Angle (degree) · 3Outer Diameter (Millimeter) · 1Length (Meter) · 1

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

How many water jet knife system handpiece, single-use products are registered in the US?

57 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Water jet knife system handpiece, single-use", from 4 companies. The largest labeler is Hydrocision, Inc. with 56% of records.

Which FDA product codes apply?

HRX (Arthroscope), FQH (Lavage, Jet), FQH (LAVAGE, JET), PZP (Fluid jet removal system)

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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