A hand-held, manual tubular device designed as an interface between an ophthalmic cannula intended for infusion, irrigation and/or aspiration (e.g., a capsular polishing or a cystotome cannula) and associated tubing, to facilitate manipulation of the cannula.
| Company | Devices | Share |
|---|---|---|
| Oasis Medical, Inc. | 40 | 62% |
| Psi/Eye-Ko, Inc. | 17 | 26% |
| Sterimedix Limited | 3 | 5% |
| Aktive Srl | 3 | 5% |
| Vitreq B.V. | 2 | 3% |
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 |
|---|---|---|
| HMX | Cannula, Ophthalmic | 42 |
| KYG | Device, Irrigation, Ocular Surgery | 17 |
| MED | Sterilant, Medical Devices | 3 |
| HNY | Cystotome | 3 |
Use these as the dimensions to specify in a tender line.
65 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Ophthalmic surgical irrigation/infusion/aspiration handle, single-use", from 5 companies. The largest labeler is Oasis Medical, Inc. with 62% of records.
HMX (Cannula, Ophthalmic), KYG (Device, Irrigation, Ocular Surgery), MED (Sterilant, Medical Devices), HNY (Cystotome)
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.