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Device Explorer · FDA GUDID · GMDN 47806

Laryngoscope handle, single-use

A clean, non-sterile, hand-held segment of a laryngoscope (i.e., non-endoscopic rigid type) designed to manipulate the laryngoscope blade during airway access and intubation. It is a cylindrical device that contains batteries/light-emitting cells to provide th

US‑registered devices75in commercial distribution
Companies15labelers on GUDID
Single‑use96%of device records
Sterile21%labelled sterile
Prescription55%Rx‑only share
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Share of device records

Carnegie Surgical Llc1216%
Proact Medical Limited1115%
Teleflex Incorporated1013%
Salter Labs68%
Maco International68%
Flexicare Medical Limited57%
Timesco Healthcare Limited45%
Novamed-Usa Inc.45%

Top labelers

CompanyDevicesShare
Carnegie Surgical Llc1216%
Proact Medical Limited1115%
Teleflex Incorporated1013%
Salter Labs68%
Maco International68%
Flexicare Medical Limited57%
Timesco Healthcare Limited45%
Novamed-Usa Inc.45%
Bound Tree Medical, Llc45%
Sunmed, Llc45%
Prestige Ameritech, Ltd.34%
Biomet Orthopedics, Llc23%

Company = labeler of record on GUDID. 15 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

Britepro Solo Single-Use Fiber Optic LaryngoscopSingle-Use Conventional Laryngoscope HandleBritePro Handle Single-Use Fiber OpticBritepro Solo Mini Single-Use Fiber Optic LaryngBritePro Solo Evo Single-Use Fiber Optic LaryngoCallisto Single-Use LaryngoscopesPenlonDISPOSABLE FIBER OPTIC MCINTOSH BLADE ADULT# 3Reconstructive WedgeRECONSTRUCTIVE WEDGEPremierProNOVALITECuraplexIntuBrite SterilePROACT MR ConditionalPROACT Metal Max

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

FDA product codes

CodeNameDevices
CCWLaryngoscope, Rigid53
CCWLARYNGOSCOPE, RIGID20
HRSPlate, fixation, bone2
HWCScrew, fixation, bone2

GMDN & GCC registration

  • GMDN code 47806 · non‑implantable
  • Single‑use 96% · sterile 21% · Rx‑only 55% · 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 laryngoscope handle, single-use products are registered in the US?

75 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Laryngoscope handle, single-use", from 15 companies. The largest labeler is Carnegie Surgical Llc with 16% of records.

Which FDA product codes apply?

CCW (Laryngoscope, Rigid), CCW (LARYNGOSCOPE, RIGID), HRS (Plate, fixation, bone), HWC (Screw, fixation, bone)

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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