Consulting Wallah › Device Explorer › Catheters & tubes › Basic endotracheal tube, single-use
Device Explorer · FDA GUDID · GMDN 46967

Basic endotracheal tube, single-use

A hollow cylinder inserted orally or nasally into the trachea to provide an unobstructed airway to convey gases and vapours to and from the lungs during anaesthesia, resuscitation, and other situations where the patient is not properly ventilated; it does not

US‑registered devices2,720in commercial distribution
Companies34labelers on GUDID
Single‑use100%of device records
Sterile99%labelled sterile
Prescription82%Rx‑only share
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Share of device records

Teleflex Incorporated48418%
Covidien Lp31211%
Salter Labs29211%
Flexicare Medical Limited1746%
Well Lead Medical Co.,Ltd1526%
Sourcemark, Llc.1485%
Bound Tree Medical, Llc1475%
Sunmed, Llc1405%

Top labelers

CompanyDevicesShare
Teleflex Incorporated48418%
Covidien Lp31211%
Salter Labs29211%
Flexicare Medical Limited1746%
Well Lead Medical Co.,Ltd1526%
Sourcemark, Llc.1485%
Bound Tree Medical, Llc1475%
Sunmed, Llc1405%
Icu Medical, Inc.1335%
Kentron Healthcare, Inc.1094%
Medline Industries, Inc.964%
Forsure Medical Products Llc713%

Company = labeler of record on GUDID. 34 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

AnapnoGuard™ Endotracheal Tube 8.0mmAnapnoGuard™ Endotracheal Tube 7.5mmAnapnoGuard™ Endotracheal Tube 7.0mmTRACHEOSCOPIC VENTILATION TUBE ASVivaSight-SLGOBENEndotracheal Tube with Evacuation LumenWell Lead Endotracheal TubeWell Lead Endotracheal Tube with Evacuation LumeMedisLMAVENTISEAL ORAL/NASAL (ON) ET TUBE ID 3.0 MAGILL PLAIN ORAL/NASAL(ON)ET TUBE ID 2.5 MAGILL - STERPLAIN ORAL/NASAL(ON)ET TUBE ID 2.5 - STERILE USPLAIN ORAL/NASAL(ON)ET TUBE ID 3.0 MAGILL - STERPLAIN ORAL/NASAL(ON)ET TUBE ID 3.0 - STERILE US

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

FDA product codes

CodeNameDevices
BTRTube, Tracheal (W/Wo Connector)1,518
BTRTube, tracheal (w/wo connector)1,443
ETNSTIMULATOR, NERVE42
CBKVentilator, continuous, facility use13
BSYCatheters, Suction, Tracheobronchial7
LNZChanger, tube, endotracheal4

GMDN & GCC registration

  • GMDN code 46967 · non‑implantable
  • Single‑use 100% · sterile 99% · Rx‑only 82% · OTC 1%
  • UAE: MOHAP / DoH medical device registration and an authorised representative are required; Saudi: SFDA MDMA. We check status on request.

Size attributes recorded

Lumen/Inner Diameter (Millimeter) · 657Outer Diameter (Millimeter) · 638Length (Millimeter) · 381Height (Millimeter) · 173Width (Millimeter) · 172Catheter Inner Diameter (Millimeter) · 6

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

How many basic endotracheal tube, single-use products are registered in the US?

2,720 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Basic endotracheal tube, single-use", from 34 companies. The largest labeler is Teleflex Incorporated with 18% of records.

Which FDA product codes apply?

BTR (Tube, Tracheal (W/Wo Connector)), BTR (Tube, tracheal (w/wo connector)), ETN (STIMULATOR, NERVE), CBK (Ventilator, continuous, facility use)

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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