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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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EisPack — 4 UDI-DI variants, MDR (Schupp GmbH & Co. KG)

MD Atlas
Schupp GmbH & Co. KG

Data from EUDAMED, last updated May 23, 2026

EisPack

402788719EisPACKE6

4 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: Schupp GmbH & Co. KG

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 402788719EisPACKE6
Device name: EisPack
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 15, 2025

Manufacturer & authorised representative

Manufacturer

Name: Schupp GmbH & Co. KG
SRN: DE-MF-000010127
Country: Germany
Email: zentrale@schupp-gmbh.de
Phone: +49 7443 2430

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01JVA4ZJCM8KDRQQR8E5SYSPRE

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

191904027887019198
192004027887019204
192104027887019211
192204027887019228