A device intended to be fitted to an endoscope suction channel to enable the operator to control suction whist preventing inflow of air. It is in the form of an attachable valve that controls (opens/closes) the suction channel. This is a reusable device.
| Company | Devices | Share |
|---|---|---|
| Hoya Corporation | 14 | 20% |
| Pentax Medical Corporation | 14 | 20% |
| Olympus Medical Systems Corp. | 9 | 13% |
| Dufner - Instrumente Gmbh Fabrik Ärztlicher Instrumente Medizintechnik | 8 | 11% |
| Karl Storz Gmbh & Co. Kg | 6 | 9% |
| Olympus Winter & Ibe Gmbh | 6 | 9% |
| Fujifilm Corporation | 4 | 6% |
| Pentax Of America, Inc. | 3 | 4% |
| Allied Medical, Llc | 3 | 4% |
| Sontec Instruments, Inc. | 2 | 3% |
| Anrei Medical(Hz) Co.,Ltd. | 1 | 1% |
Company = labeler of record on GUDID. 11 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 |
|---|---|---|
| GCJ | Laparoscope, General & Plastic Surgery | 25 |
| FDS | Gastroscope And Accessories, Flexible/Rigid | 6 |
| EOQ | Bronchoscope (Flexible Or Rigid) | 6 |
| EOQ | BRONCHOSCOPE (FLEXIBLE OR RIGID) | 6 |
| FDS | Gastroscope and accessories, flexible/rigid | 6 |
| FDF | Colonoscope and accessories, flexible/rigid | 5 |
Use these as the dimensions to specify in a tender line.
70 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endoscope suction valve, reusable", from 11 companies. The largest labeler is Hoya Corporation with 20% of records.
GCJ (Laparoscope, General & Plastic Surgery), FDS (Gastroscope And Accessories, Flexible/Rigid), EOQ (Bronchoscope (Flexible Or Rigid)), EOQ (BRONCHOSCOPE (FLEXIBLE OR RIGID))
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.