A sterile endoscope with a flexible inserted portion intended for the visual examination and treatment of the bladder and the urinary tract by introduction through the urethra. Anatomical images are transmitted from a distal camera and displayed on a monitor.
| Company | Devices | Share |
|---|---|---|
| Hunan Vathin Medical Instrument Co., Ltd | 28 | 19% |
| Otu Medical Inc. | 22 | 15% |
| Medimaging Integrated Solution Inc. | 17 | 11% |
| Prosurg Inc | 17 | 11% |
| Macrolux Medical Technology Co., Ltd. | 14 | 9% |
| Ningbo Wise Optomech Technology Corporation | 12 | 8% |
| Ambu A/S | 7 | 5% |
| Shenzhen Hugemed Medical Technical Development Co., Ltd. | 6 | 4% |
| Shanghai Seegen Photoelectric Technology Co.,Ltd. (Yindu Road Factory) | 4 | 3% |
| Zhuhai Pusen Medical Technology Co, Ltd | 4 | 3% |
| Shanghai Anqing Medical Instrument Co., Ltd | 4 | 3% |
| Guangzhou Red Pine Medical Instrument Co., Ltd. | 2 | 1% |
Company = labeler of record on GUDID. 19 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 |
|---|---|---|
| FAJ | Cystoscope And Accessories, Flexible/Rigid | 135 |
| FGB | Ureteroscope And Accessories, Flexible/Rigid | 16 |
| FAJ | Cystoscope and accessories, flexible/rigid | 9 |
| FAS | Electrode, Electrosurgical, Active, Urological | 1 |
| MNL | Accessories, Cleaning Brushes, For Endoscope | 1 |
Use these as the dimensions to specify in a tender line.
148 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Flexible video cystoscope, single-use", from 19 companies. The largest labeler is Hunan Vathin Medical Instrument Co., Ltd with 19% of records.
FAJ (Cystoscope And Accessories, Flexible/Rigid), FGB (Ureteroscope And Accessories, Flexible/Rigid), FAJ (Cystoscope and accessories, flexible/rigid), FAS (Electrode, Electrosurgical, Active, Urological)
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.