Consulting Wallah › Device Explorer › Syringes, needles & infusion › Pleuroscopic/mediastinoscopic access cannula, reus
Device Explorer · FDA GUDID · GMDN 62857

Pleuroscopic/mediastinoscopic access cannula, reusable

A rigid, single-lumen, surgical instrument intended to be percutaneously inserted through the chest to provide access to the pleural and/or mediastinal cavity to facilitate the introduction of surgical instruments as part of a minimally-invasive procedure; it

US‑registered devices50in commercial distribution
Companies6labelers on GUDID
Single‑use2%of device records
Sterile2%labelled sterile
Prescription56%Rx‑only share
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Share of device records

Karl Storz Gmbh & Co. Kg2040%
Landanger1734%
Wexler Surgical, Inc.510%
Genesee Biomedical, Inc.48%
Lsi Solutions, Inc.36%
Atricure, Inc.12%

Top labelers

CompanyDevicesShare
Karl Storz Gmbh & Co. Kg2040%
Landanger1734%
Wexler Surgical, Inc.510%
Genesee Biomedical, Inc.48%
Lsi Solutions, Inc.36%
Atricure, Inc.12%

Company = labeler of record on GUDID. 6 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

n.a.DELACROIX-CHEVALIERminiARM® multiSTATION™ SystemmultiSTATION™Wexler Surgical, Inc.Thoracic Port with Obturator 18x90mmThoracic Port with Obturator 18x70mmThoracic Port with Obturator 18x50mmThoracic Port with Obturator 18x110mmSubtle Cannula with Guide

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

FDA product codes

CodeNameDevices
DWSInstruments, Surgical, Cardiovascular21
GCJLaparoscope, general & plastic surgery20
GEACannula, Surgical, General & Plastic Surgery5
GEACANNULA, SURGICAL, GENERAL & PLASTIC SURGERY2
MDMINSTRUMENT, MANUAL, SURGICAL, GENERAL USE1
OCMSurgical Cardiac Ablation Device, For Treatment Of Atrial Fi1

GMDN & GCC registration

  • GMDN code 62857 · non‑implantable
  • Single‑use 2% · sterile 2% · Rx‑only 56% · 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 (Centimeter) · 1

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

No closely related category with 50+ devices.

How many pleuroscopic/mediastinoscopic access cannula, reusable 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 "Pleuroscopic/mediastinoscopic access cannula, reusable", from 6 companies. The largest labeler is Karl Storz Gmbh & Co. Kg with 40% of records.

Which FDA product codes apply?

DWS (Instruments, Surgical, Cardiovascular), GCJ (Laparoscope, general & plastic surgery), GEA (Cannula, Surgical, General & Plastic Surgery), GEA (CANNULA, SURGICAL, 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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