An endoscope with a rigid inserted portion intended for the visual examination and treatment of the nasal cavity and/or nasopharynx. It is inserted into the body through a nostril or the oral cavity during rhinoscopy or an ear/nose/throat (ENT) intervention. A
| Company | Devices | Share |
|---|---|---|
| Karl Storz Gmbh & Co. Kg | 56 | 56% |
| Stryker Corporation | 20 | 20% |
| Olympus Winter & Ibe Gmbh | 16 | 16% |
| Schölly Fiberoptic Gmbh | 7 | 7% |
| Rz-Medizintechnik Gmbh | 1 | 1% |
Company = labeler of record on GUDID. 5 companies in total; top 12 shown. Click headers to sort.
Sample of brand names as labelled; no endorsement. Ask us for the full list with company, model and UDI.
| Code | Name | Devices |
|---|---|---|
| EOB | NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID) | 56 |
| EOB | Nasopharyngoscope (Flexible Or Rigid) | 22 |
| EOB | Nasopharyngoscope (flexible or rigid) | 20 |
| EQL | Laryngostroboscope | 2 |
| HRX | Arthroscope | 1 |
Use these as the dimensions to specify in a tender line.
100 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Rigid optical rhinoscope", from 5 companies. The largest labeler is Karl Storz Gmbh & Co. Kg with 56% of records.
EOB (NASOPHARYNGOSCOPE (FLEXIBLE OR RIGID)), EOB (Nasopharyngoscope (Flexible Or Rigid)), EOB (Nasopharyngoscope (flexible or rigid)), EQL (Laryngostroboscope)
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.
Add rigid optical rhinoscope to the RFQ basket or use the form below with quantity, specification and delivery location; the Network returns comparable quotes from verified suppliers in 2–5 working days.
Hospitals, pharmacies and distributors anywhere: tell us what you need and the Consulting Wallah Network returns comparable quotes from verified suppliers. No fee for buyers.
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.