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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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Lokosana — 7 UDI-DI variants, MDR

MD Atlas
SAMINA Produktions- und Handels GmbH

Data from EUDAMED, last updated May 23, 2026

Lokosana

912009641LOKGZ

7 UDI-DI variants

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

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Manufacturer: SAMINA Produktions- und Handels GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 912009641LOKGZ
Device name: —
Device model: Lokosana
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Sep 12, 2023

Manufacturer & authorised representative

Manufacturer

Name: SAMINA Produktions- und Handels GmbH
SRN: AT-MF-000037511
Country: Austria
Email: sabrina.amann@samina.com

Variants by status

UDI-DI variants

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01HA4EJ89FQX1G5SNYJV0H182K

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

1265209120096410086
1331909120096410093
1332009120096410109
1029209120096410116
1265109120096410055
1265009120096410062
1157509120096410079