A device that is attached to a dedicated handpiece for insertion into the eye to deliver energy (e.g., ultrasonic, piezoelectric), provided from a system generator, to perform phacoemulsification (a procedure for the liquefying and removal of the opaque lens n
| Company | Devices | Share |
|---|---|---|
| D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. | 39 | 36% |
| Bausch & Lomb Incorporated | 24 | 22% |
| Alcon Laboratories, Inc. | 17 | 16% |
| Johnson & Johnson Surgical Vision, Inc. | 16 | 15% |
| Oertli-Instrumente Ag | 10 | 9% |
| Microvision, Inc. | 1 | 1% |
Company = labeler of record on GUDID. 6 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 |
|---|---|---|
| HQC | Unit, Phacofragmentation | 74 |
| HQC | Unit, phacofragmentation | 38 |
| HQE | Instrument, Vitreous Aspiration And Cutting, Ac-Powered | 3 |
Use these as the dimensions to specify in a tender line.
107 device records in commercial distribution are listed on the FDA Global Unique Device Identification Database (GUDID) under the GMDN category "Phacoemulsification system handpiece tip, single-use", from 6 companies. The largest labeler is D.O.R.C. Dutch Ophthalmic Research Center (International) B.V. with 36% of records.
HQC (Unit, Phacofragmentation), HQC (Unit, phacofragmentation), HQE (Instrument, Vitreous Aspiration And Cutting, Ac-Powered)
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.