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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Phacoemulsification/ Vitrectomy System — 3 UDI-DI variants, MDR

MD Atlas
VitreQ B.V.

Data from EUDAMED, last updated May 31, 2026

Phacoemulsification/ Vitrectomy System

871921422994GQ

3 UDI-DI variants

MDR [Regulation (EU) 2017/745 on medical devices]Class IIb

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: VitreQ B.V.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 871921422994GQ
Device name: Phacoemulsification/ Vitrectomy System
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: May 26, 2026

Manufacturer & authorised representative

Manufacturer

Name: VitreQ B.V.
SRN: NL-MF-000000424
Country: Netherlands
Email: infovitreq@bvimedical.com

Variants by status

UDI-DI variants

3 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KRZGTZ8F7E1BKFVM871XMEKP

Format

Summary

29 columns included

Trade name
Basic UDI-DI
UDI-DI code
Risk category
Applicable legislation
Status
Organization name
SRN
Reference / catalog number
Additional product description
Intended medical purpose
Placed on the market (country)
Market info update date
Sterile
Single use
Contains latex
Reprocessed single-use
Direct marking
CMR substance
Endocrine disruptor
Annex XVI applicable
Sterilization
OEM applicable
EMDN codes
Last updated
Basic UDI-DI device name
Basic UDI-DI device model
Basic UDI-DI implantable
Basic UDI-DI reagent

EQ00.R0308719214223656
EQ00.R0108719214223632
EQ00.R0208719214223649