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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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MSK Eye — 1 UDI-DI variant, MDR (Oxipit, UAB)

MD Atlas
Oxipit, UAB

Data from EUDAMED, last updated May 31, 2026

MSK Eye

477905043MSKEYEPV

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Manufacturer: Oxipit, UAB

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 477905043MSKEYEPV
Device name: MSK Eye
Device model: MSK Eye
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIb
Special device type: refdata.special-mdr-device-type.software
Version date: Feb 5, 2026

Manufacturer & authorised representative

Manufacturer

Name: Oxipit, UAB
SRN: LT-MF-000022304
Country: Lithuania
Email: info@oxipit.ai
Phone: +37062599148

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01KGPYRQ5JX32DMMS5XANMDXHP

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

MSK Eye04779050430124