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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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LiNA Versascope Outflow Cannula — 1 UDI-DI variant, MDR

MD Atlas
LiNA Medical ApS

Data from EUDAMED, last updated May 31, 2026

LiNA Versascope Outflow Cannula

57082651023-1APL

1 UDI-DI variant

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: LiNA Medical ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57082651023-1APL
Device name: LiNA Versascope Outflow Cannula
Device model: GMS 720
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 30, 2023

Manufacturer & authorised representative

Manufacturer

Name: LiNA Medical ApS
SRN: DK-MF-000003706
Country: Denmark
Email: plu@lina-medical.com
Phone: +48 789 105 422

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01H46824A1J49RN5M2YKBJGD4Z

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

GMS 70205708265013562