A flexible fibreoptic cable that is designed to transport cold light from a light source to an instrument or other equipment, e.g., an endoscope or a headlight. The fibreoptic bundle is protected within a sheath and can be made of either glass or plastic fibre
| Company | Devices | Share |
|---|---|---|
| Surgical Direct, Inc. | 268 | 25% |
| Karl Storz Gmbh & Co. Kg | 88 | 8% |
| Jedmed Instrument Company | 80 | 8% |
| Gulf Fiberoptics, Inc. | 77 | 7% |
| Elmed Incorporated | 60 | 6% |
| Teleflex Incorporated | 45 | 4% |
| Ambler Surgical Corp. | 40 | 4% |
| Lumitex, Inc. | 36 | 3% |
| Rz-Medizintechnik Gmbh | 24 | 2% |
| Fentex Medical Gmbh | 23 | 2% |
| Black & Black Surgical, Inc. | 21 | 2% |
| Accurate Surgical & Scientific Instruments Corporation | 20 | 2% |
Company = labeler of record on GUDID. 65 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 |
|---|---|---|
| FFS | Image, Illumination, Fiberoptic, For Endoscope | 296 |
| EQH | Source, Carrier, Fiberoptic Light | 225 |
| EQH | SOURCE, CARRIER, FIBEROPTIC LIGHT | 136 |
| FCW | Light source, fiberoptic, routine | 91 |
| HBI | Illuminator, Fiberoptic, Surgical Field | 87 |
| FFS | image, illumination, fiberoptic, for endoscope | 72 |
Use these as the dimensions to specify in a tender line.
1,059 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Fibreoptic light cable, reusable", from 65 companies. The largest labeler is Surgical Direct, Inc. with 25% of records.
FFS (Image, Illumination, Fiberoptic, For Endoscope ), EQH (Source, Carrier, Fiberoptic Light), EQH (SOURCE, CARRIER, FIBEROPTIC LIGHT), FCW (Light source, fiberoptic, routine)
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.