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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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Opthalmic Viscosurgical Device — 12 UDI-DI variants, MDR (Phibio GmbH)

MD Atlas
Phibio GmbH

Data from EUDAMED, last updated May 23, 2026

Opthalmic Viscosurgical Device

425090620HA-OVDUG

12 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: Phibio GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 425090620HA-OVDUG
Device name: Opthalmic Viscosurgical Device
Device model: Opthalmic Viscosurgical Device
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Version date: Aug 27, 2025

Manufacturer & authorised representative

Manufacturer

Name: Phibio GmbH
SRN: DE-MF-000045435
Country: Germany
Email: info@phibio.de
Phone: ‎+49 162 3468981

Variants by status

UDI-DI variants

12 UDI-DI variants

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Applied filters

basicUdiUlid01K3N3FZZNZZN7DN1ETPRP0X2Y

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

ViscOge04250906200127
ViscOge04250906200134
ViscOge04250906200158
ViscOge04250906200110
ViscOge04250906200141
ViscOge04250906200165
VisOcu04250906200073
VisOcu04250906200066
VisOcu04250906200035
VisOcu04250906200080
VisOcu04250906200059
VisOcu04250906200042