An electrically-powered device designed to receive and process the electronic signals sent from a video endoscope or endoscopic video camera; it does not include the endoscope nor light source and is not designed to control the endoscope. It may have additiona
| Company | Devices | Share |
|---|---|---|
| Pentax Of America, Inc. | 47 | 16% |
| Karl Storz Gmbh & Co. Kg | 22 | 7% |
| Scivita Medical Technology Co., Ltd. | 19 | 6% |
| Santa Barbara Imaging Systems, Inc. | 19 | 6% |
| Macrolux Medical Technology Co., Ltd. | 18 | 6% |
| Nds Surgical Imaging Llc | 14 | 5% |
| Hoya Corporation | 13 | 4% |
| Zhuhai Pusen Medical Technology Co, Ltd | 11 | 4% |
| Otu Medical Inc. | 10 | 3% |
| Ningbo Wise Optomech Technology Corporation | 8 | 3% |
| Pentax Medical Corporation | 8 | 3% |
| Boston Scientific Corporation | 8 | 3% |
Company = labeler of record on GUDID. 49 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 |
|---|---|---|
| LMB | Device, Digital Image Storage, Radiological | 91 |
| PEA | Endoscope, Accessories, Image Post-Processing For Color Enha | 47 |
| EOQ | Bronchoscope (Flexible Or Rigid) | 45 |
| GCJ | Laparoscope, General & Plastic Surgery | 42 |
| FET | Endoscopic video imaging system/component, gastroenterology- | 36 |
| FGB | Ureteroscope And Accessories, Flexible/Rigid | 28 |
Use these as the dimensions to specify in a tender line.
299 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Endoscopic video image processing unit", from 49 companies. The largest labeler is Pentax Of America, Inc. with 16% of records.
LMB (Device, Digital Image Storage, Radiological), PEA (Endoscope, Accessories, Image Post-Processing For Color Enha), EOQ (Bronchoscope (Flexible Or Rigid)), GCJ (Laparoscope, General & Plastic Surgery)
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.