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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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Geysir — 3 UDI-DI variants, MDR (LISCHKA GmbH)

MD Atlas
LISCHKA GmbH

Data from EUDAMED, last updated May 23, 2026

Geysir

426068755GEYSIRHZ

3 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: LISCHKA GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426068755GEYSIRHZ
Device name: Geysir
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 15, 2024

Manufacturer & authorised representative

Manufacturer

Name: LISCHKA GmbH
SRN: DE-MF-000018110
Country: Germany
Email: stefan.lischka@lischka.berlin
Phone: +49 30 98 19 58 125

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01JA7QM738NR95CNJ33CKDX8KE

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

09040004260687550502
09040304260687550601
09040604260687550908