Consulting Wallah › Device Explorer › Catheters & tubes › Reinforced endotracheal tube, single-use
Device Explorer · FDA GUDID · GMDN 46569

Reinforced endotracheal tube, single-use

An armoured 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

US‑registered devices291in commercial distribution
Companies12labelers on GUDID
Single‑use100%of device records
Sterile100%labelled sterile
Prescription83%Rx‑only share
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Share of device records

Teleflex Incorporated12443%
Flexicare Medical Limited3813%
Forsure Medical Products Llc3010%
Well Lead Medical Co.,Ltd248%
Medtronic Xomed, Inc.228%
Icu Medical, Inc.155%
Salter Labs145%
Venner Medical (Singapore) Pte. Ltd.83%

Top labelers

CompanyDevicesShare
Teleflex Incorporated12443%
Flexicare Medical Limited3813%
Forsure Medical Products Llc3010%
Well Lead Medical Co.,Ltd248%
Medtronic Xomed, Inc.228%
Icu Medical, Inc.155%
Salter Labs145%
Venner Medical (Singapore) Pte. Ltd.83%
Medline Industries, Inc.72%
Tianjin Medis Medical Device Co.,Ltd.41%
Fuji Systems Corporation31%
Endure Industries21%

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

Brand names on the register (sample)

Reinforced Endotracheal TubeMedisPLAIN REINFORCED ET TUBE ID 3.0 - STERILEPLAIN REINFORCED ET TUBE ID 3.5 - STERILEPLAIN REINFORCED ET TUBE ID 4.0 - STERILEPLAIN REINFORCED ET TUBE ID 4.5 - STERILE- USAPLAIN REINFORCED ET TUBE ID 5.0 - STERILE- USAPLAIN REINFORCED ET TUBE ID 5.5 - STERILE- USAPLAIN REINFORCED ET TUBE ID 6.0 - STERILE- USAPLAIN REINFORCED ET TUBE ID 6.5 - STERILE-USAPLAIN REINFORCED ET TUBE ID 7.0 - STERILEPLAIN REINFORCED ET TUBE ID 7.5 - STERILEPLAIN REINFORCED ET TUBE ID 8.0 - STERILEPLAIN REINFORCED ET TUBE ID 8.5 - STERILEPLAIN REINFORCED ET TUBE ID 9.0 - STERILEVENTISEAL REINFORCED ET TUBE ID 5.0 - STERILE -

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)146
BTRTube, Tracheal (W/Wo Connector)123
ETNSTIMULATOR, NERVE25

GMDN & GCC registration

  • GMDN code 46569 · non‑implantable
  • Single‑use 100% · sterile 100% · Rx‑only 83% · 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

Lumen/Inner Diameter (Millimeter) · 91Outer Diameter (Millimeter) · 68Length (Millimeter) · 58Height (Millimeter) · 28Width (Millimeter) · 28Catheter Inner Diameter (Millimeter) · 4

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

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

291 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Reinforced endotracheal tube, single-use", from 12 companies. The largest labeler is Teleflex Incorporated with 43% of records.

Which FDA product codes apply?

BTR (Tube, tracheal (w/wo connector)), BTR (Tube, Tracheal (W/Wo Connector)), ETN (STIMULATOR, NERVE)

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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