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Device Explorer · FDA GUDID · GMDN 36653

Rigid optical oesophagoscope

An endoscope with a rigid inserted portion intended for the visual examination and treatment of the oesophagus. It is inserted into the body through the mouth. Anatomical images are transmitted to the user through relayed lens optics or a fibreoptic bundle. Th

US‑registered devices102in commercial distribution
Companies4labelers on GUDID
Single‑use0%of device records
Sterile0%labelled sterile
Prescription99%Rx‑only share
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Share of device records

Teleflex Incorporated6665%
Karl Storz Gmbh & Co. Kg3231%
Integra Microfrance33%
Sizewise Rentals, L.L.C.11%

Top labelers

CompanyDevicesShare
Teleflex Incorporated6665%
Karl Storz Gmbh & Co. Kg3231%
Integra Microfrance33%
Sizewise Rentals, L.L.C.11%

Company = labeler of record on GUDID. 4 companies in total; top 12 shown. Click headers to sort.

Brand names on the register (sample)

n.a.SizewisePILLINGMicroFrance®

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

FDA product codes

CodeNameDevices
EOXESOPHAGOSCOPE (FLEXIBLE OR RIGID)70
EOXEsophagoscope (flexible or rigid)31
EOQBRONCHOSCOPE (FLEXIBLE OR RIGID)5
EPYSPECULUM, ENT4
CCWLARYNGOSCOPE, RIGID3
FEMACCESSORIES, PHOTOGRAPHIC, FOR ENDOSCOPE (EXCLUDE LIGHT SOUR1

GMDN & GCC registration

  • GMDN code 36653 · non‑implantable
  • Single‑use 0% · sterile 0% · Rx‑only 99% · 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) · 62Width (Millimeter) · 60Lumen/Inner Diameter (Millimeter) · 4Length (Inch) · 4

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

How many rigid optical oesophagoscope products are registered in the US?

102 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid optical oesophagoscope", from 4 companies. The largest labeler is Teleflex Incorporated with 65% of records.

Which FDA product codes apply?

EOX (ESOPHAGOSCOPE (FLEXIBLE OR RIGID)), EOX (Esophagoscope (flexible or rigid)), EOQ (BRONCHOSCOPE (FLEXIBLE OR RIGID)), EPY (SPECULUM, ENT)

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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