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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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Sterile Ophthalmic Surgical Procedure… — 10 UDI-DI variants, MDR

MD Atlas
VitreQ B.V.

Data from EUDAMED, last updated May 31, 2026

Sterile Ophthalmic Surgical Procedure Pack

871921422995GS

10 UDI-DI variants

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

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

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 871921422995GS
Device name: Sterile Ophthalmic Surgical Procedure Pack
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
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

10 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KS01GQNA3HXC02P1NCZYPZN8

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

PA20.D0108719214223960
PA21.D0208719214223991
PA00.D0208719214223489
PA22.D0208719214224011
PA22.D0108719214224004
PA21.D0108719214223984
PA25.D0108719214223519
PA27.D0108719214223533
PA20.D0208719214223977
PA23.D0108719214223496