Consulting Wallah › Device Explorer › Other devices › Rigid intubation laryngoscope, single-use
Device Explorer · FDA GUDID · GMDN 62918

Rigid intubation laryngoscope, single-use

A hand-held disposable device intended to be used by anaesthesia/emergency service personnel to manipulate the tongue, preventing it from obstructing the oropharynx and enabling a clear view of the trachea for the insertion of an endotracheal (ET) tube prior t

US‑registered devices332in commercial distribution
Companies11labelers on GUDID
Single‑use100%of device records
Sterile64%labelled sterile
Prescription53%Rx‑only share
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Share of device records

Flexicare Medical Limited12939%
Provision5918%
Medsource International Llc5216%
Carnegie Surgical Llc3912%
Bound Tree Medical, Llc288%
Timesco Healthcare Limited113%
Prestige Ameritech, Ltd.93%
Adroit Surgical21%

Top labelers

CompanyDevicesShare
Flexicare Medical Limited12939%
Provision5918%
Medsource International Llc5216%
Carnegie Surgical Llc3912%
Bound Tree Medical, Llc288%
Timesco Healthcare Limited113%
Prestige Ameritech, Ltd.93%
Adroit Surgical21%
Zhuhai Pusen Medical Technology Co, Ltd10%
Enter Medical Corporation10%
North American Rescue, Llc10%

Company = labeler of record on GUDID. 11 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Single-use Video LaryngoscopeBritePro OmniBritePro SoloBritePro Solo Evo Single-Use Fiber Optic Handle BritePro Omni Single-Use Laryngoscope Mini HandlBritePro Omni Single-Use Laryngoscope Mini HandlBritePro Omni Single-Use Laryngoscope Mini HandlBritePro Omni Single-Use Laryngoscope Mini HandlBritePro Omni Single-Use Laryngoscope Handle WitBritePro Omni Single-Use Laryngoscope Handle WitBritePro Omni Single-Use Laryngoscope Handle WitOmni Integrated Single Use Laryngoscope Handle MBritePro Omni Single-Use Laryngoscope Handle WitBritePro Omni Single-Use Laryngoscope Handle WitBritePro Omni Single-Use Laryngoscope Handle WitBritePro Omni Single-Use Laryngoscope Handle Wit

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

FDA product codes

CodeNameDevices
CCWLaryngoscope, Rigid285
CCWLARYNGOSCOPE, RIGID27
GAHStylet, Surgical, General & Plastic Surgery12
OGHLaryngoscope kit1
OGKOrotracheal intubation guide kit1
LNZChanger, tube, endotracheal1

GMDN & GCC registration

  • GMDN code 62918 · non‑implantable
  • Single‑use 100% · sterile 64% · Rx‑only 53% · 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

No structured size data on the register.

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

How many rigid intubation laryngoscope, single-use products are registered in the US?

332 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid intubation laryngoscope, single-use", from 11 companies. The largest labeler is Flexicare Medical Limited with 39% of records.

Which FDA product codes apply?

CCW (Laryngoscope, Rigid), CCW (LARYNGOSCOPE, RIGID), GAH (Stylet, Surgical, General & Plastic Surgery), OGH (Laryngoscope kit)

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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