Consulting Wallah › Device Explorer › Catheters & tubes › Cuff-suction endotracheal tube
Device Explorer · FDA GUDID · GMDN 47691

Cuff-suction endotracheal tube

A hollow cylinder inserted orally into the trachea to maintain airway patency, typically for patients anticipated to require prolonged mechanical ventilation in critical care, that enables removal of pooled secretion above its distal cuff with suction. It cons

US‑registered devices89in commercial distribution
Companies8labelers on GUDID
Single‑use99%of device records
Sterile99%labelled sterile
Prescription100%Rx‑only share
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Share of device records

Covidien Lp2831%
Teleflex Incorporated2528%
Salter Labs1416%
Medline Industries, Inc.89%
Icu Medical, Inc.78%
Tianjin Medis Medical Device Co.,Ltd.56%
Widex A/S11%
Avanos Medical, Inc.11%

Top labelers

CompanyDevicesShare
Covidien Lp2831%
Teleflex Incorporated2528%
Salter Labs1416%
Medline Industries, Inc.89%
Icu Medical, Inc.78%
Tianjin Medis Medical Device Co.,Ltd.56%
Widex A/S11%
Avanos Medical, Inc.11%

Company = labeler of record on GUDID. 8 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

MedisWidexTELEFLEXShileyMallinckrodtPortexRUSCHMedline Industries, Inc.Parker Flex-TipHalyard

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)72
BTRTube, Tracheal (W/Wo Connector)24
OSMHearing aid, air conduction with wireless technology1
NTRIMMUNOHISTOCHEMICAL REAGENT, ANTIBODY (MONOCLONAL OR POLYCLO1

GMDN & GCC registration

  • GMDN code 47691 · non‑implantable
  • Single‑use 99% · sterile 99% · 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 (Millimeter) · 19Lumen/Inner Diameter (Millimeter) · 14Outer Diameter (Millimeter) · 7Catheter Inner Diameter (Millimeter) · 5

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

How many cuff-suction endotracheal tube products are registered in the US?

89 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Cuff-suction endotracheal tube", from 8 companies. The largest labeler is Covidien Lp with 31% of records.

Which FDA product codes apply?

BTR (Tube, tracheal (w/wo connector)), BTR (Tube, Tracheal (W/Wo Connector)), OSM (Hearing aid, air conduction with wireless technology), NTR (IMMUNOHISTOCHEMICAL REAGENT, ANTIBODY (MONOCLONAL OR POLYCLO)

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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