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Device Explorer · FDA GUDID · GMDN 46840

Ophthalmic cannulation set, single-use

A collection of non-powered devices intended to be used to create a channel into the eye for posterior segment ophthalmic surgery [e.g., infusion and/or aspiration of an ophthalmic replacement medium (e.g., silicone oil)]. It consists of metal cannulae, often

US‑registered devices112in commercial distribution
Companies10labelers on GUDID
Single‑use100%of device records
Sterile98%labelled sterile
Prescription88%Rx‑only share
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Share of device records

D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.3834%
Oasis Medical, Inc.3329%
Alcon Laboratories, Inc.1412%
Mani, Inc.1211%
Medical Instrument Development Laboratories, Inc.65%
Microvision, Inc.44%
Synergetics Usa, Inc.22%
Geuder Aktiengesellschaft11%

Top labelers

CompanyDevicesShare
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.3834%
Oasis Medical, Inc.3329%
Alcon Laboratories, Inc.1412%
Mani, Inc.1211%
Medical Instrument Development Laboratories, Inc.65%
Microvision, Inc.44%
Synergetics Usa, Inc.22%
Geuder Aktiengesellschaft11%
Escalon Medical Corp.11%
Livsmed11%

Company = labeler of record on GUDID. 10 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

N.A.Viscous Fluid CannulaSurgeon's Choice CardKaiser Permanente Kit PackSurgeon's ChoiceNAAlconALCONSynergeticsMANI Infusion CannulaMANI Trocar KitMANI TrocarN/AARTISENTIAL TROCAR27G High Flow infusion line25G High Flow infusion line

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

FDA product codes

CodeNameDevices
NGYCannula, Trocar, Ophthalmic62
PZGSurgical Eye Tray33
HMXCannula, Ophthalmic14
NGYCannula, trocar, ophthalmic13
HQCUnit, phacofragmentation8
HQEInstrument, vitreous aspiration and cutting, ac-powered8

GMDN & GCC registration

  • GMDN code 46840 · non‑implantable
  • Single‑use 100% · sterile 98% · Rx‑only 88% · 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

Needle Gauge (Gauge) · 9Length (Millimeter) · 4Outer Diameter (Millimeter) · 4

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

How many ophthalmic cannulation set, single-use products are registered in the US?

112 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Ophthalmic cannulation set, single-use", from 10 companies. The largest labeler is D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. with 34% of records.

Which FDA product codes apply?

NGY (Cannula, Trocar, Ophthalmic), PZG (Surgical Eye Tray), HMX (Cannula, Ophthalmic), NGY (Cannula, trocar, ophthalmic)

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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