Ophthalmology instrumentsTherapeutic and surgical ophtholmological treatments instrumentsPhaco-vitrectomy instruments

Phaco-vitrectomy systems

EMDN code Z1212020702

9 manufacturers, 29 models including 29 on the market, 4 countries

On the market in Manufacturer country

Manufacturers registered in Europe (EUDAMED) 9

On the market
No longer marketed
93/42 Former directive, not yet certified under the MDR
Click a manufacturer to see its full range, a model to open its EUDAMED record.

Manufacturer	Country	Registered models	Class	Contact
D.O.R.C. Dutch Ophthalmic Research Center (International) FDA	Netherlands	EVA NEXUS, Phaco emulsification NCBF system93/42 EVA NEXUS, Phaco emulsification system93/42 EVA NEXUS, Phaco vitrectomy NCBF system93/42 EVA NEXUS, Phaco vitrectomy NCBF system including laser with DORC connector93/42 EVA NEXUS, Phaco vitrectomy NCBF system including laser with SMA connector93/42 13 others EVA NEXUS, Phaco vitrectomy system93/42 EVA NEXUS, Phaco vitrectomy system including laser with DORC connector93/42 EVA NEXUS, Phaco vitrectomy system including laser with SMA connector93/42 EVA, anterior machine93/42 EVA, anterior machine NCBF93/42 EVA, combined machine93/42 EVA, combined machine including Laser (DORC connector)93/42 EVA, combined machine including Laser (SMA connector)93/42 EVA, combined machine including Laser (SMA connector) with conventional Foot Pedals93/42 EVA, combined machine NCBF93/42 EVA, combined machine NCBF including Laser (DORC connector)93/42 EVA, combined machine NCBF including Laser (SMA connector)93/42 EVA, combined machine with conventional Foot Pedal93/42	IIb 93/42	Website EUDAMED record Report an error
Alcon FDA EU representative : Alcon Laboratories Belgium (Belgium)	United States	Constellation2 refs93/42 UNITY	IIb MDR, 93/42	Website regulatory-1.operations@Alcon.com EUDAMED record Report an error
Med-Logics FDA EU representative : E C REP LIMITED (Ireland)	United States	CataPulse Console93/42 CataPulse Footswitch93/42	IIb 93/42	Website EUDAMED record Report an error
Optikon 2000	Italy	12891093/42 R-EVOLUTION CR2 refs	IIb MDR, 93/42	Website EUDAMED record Report an error
BYTEC Legal Manufacturer FDA	Germany	Qube® pro Ophthalmic Surgical System 00QL0193/42	IIb 93/42	Website info@bytec-lm.com EUDAMED record Report an error
Geuder FDA	Germany	VIVOS device system3 refs	IIb MDR	Website info@geuder.de EUDAMED record Report an error
Johnson & Johnson Surgical Vision FDA EU representative : AMO Ireland (Ireland)	United States	VERITAS FOOTPEDAL3 refs	IIb MDR	Website RA-VISEU-DUVigilance@ITS.JNJ.com EUDAMED record Report an error
VitreQ FDA	Netherlands	Phacoemulsification/ Vitrectomy System EQ00.R013 refs	IIb MDR	infovitreq@bvimedical.com EUDAMED record Report an error
Zeiss FDA	Germany	QUATERA 700	IIb MDR	Website EUDAMED record Report an error

A model registered in EUDAMED is not necessarily sold in your country. Check availability and CE marking with the manufacturer.

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