Model note · Vitrectomy System
D.O.R.C. EVA NEXUS Ophthalmic Surgical System
EVA NEXUS is DORC's combined anterior and posterior segment surgical console, the successor to EVA. It uses plunger pumps acting on a cartridge for both infusion and aspiration, so the surgeon can work in flow or vacuum control, and its Smart IOP mode sets infusion pressure from the chosen aspiration and instrument data. With TDC two dimensional cutters that cut on both strokes, it reaches 20,000 cuts per minute. Options include phaco, diathermy, endoillumination and a 532 nm laser.
The model
Maker, model and type.
- Maker
- D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.
- Model
- EVA NEXUS Ophthalmic Surgical System (9000.ANTxx / COMyy)
- Device type
- Vitrectomy System
- Main document
- Open the public document
Key specifications
What the public record says.
| Item | Value | Source |
|---|---|---|
| Vitrectomy drive | Up to 10,000 cycles per minute; 20,000 cuts per minute with TDC cutters (9268 series) | Source |
| Aspiration | Plunger pump; flow 0 to 90 mL/min or vacuum 0 to -680 mmHg at sea level; rise time 300 ms | Source |
| Infusion pressure | 0 to 150 mmHg; modes Fixed, AIC and Smart IOP | Source |
| Phaco | 40 kHz, 50 W plus or minus 20 percent, stroke 80 micrometres with 3002.M handpiece | Source |
| Diathermy | 1 MHz, maximum 10 W at 100 ohm | Source |
| Endoillumination | 40 lm with 20 ga fibre; spectrum 425 to 680 nm with UV and IR filters | Source |
| Laser (optional) | 532 nm frequency doubled Nd:YAG, 0.05 to 1.2 W, 50 to 5000 ms; aiming beam 630 to 645 nm under 1 mW; Class IV | Source |
| TDC cutter sizes | 23G 0.64 mm, 25G 0.53 mm, 27G 0.43 mm shafts | Source |
| FDA clearance | K213467, product codes HQC and HQF, June 2022 | Source |
Recalls
Known FDA recalls.
- Z-2322-20262026-04-30
TDC VELOCE 23G cutters (9268.VIT23 and packs): loose outer knife complaints; 25G and 27G covered by Z-2323 and Z-2324.
FDA record
Sources
Where this note comes from.
- FDA 510(k) K213467 summary, EVA NEXUS Ophthalmic Surgical System
- openFDA recall search, D.O.R.C.
- openFDA MAUDE problem counts, brand EVA NEXUS
Not covered: DORC's user and service manuals were not publicly reachable, so there are no error codes, maintenance intervals or electrical specifications beyond the 510(k). Other DORC recalls (laser probes with Alcon/Lumenis connectors, a VGPC pack for the earlier EVA) were left out as they do not clearly apply to EVA NEXUS. The manufacturerUrl is DORC's home page and was not opened.
BMEssentia knowledge drafted from public information, reviewed by Hasan Khaled Ismail on 2026-10-24. Always follow the manufacturer's instructions for use and service manual.
Vitrectomy System
Other models of this device.
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