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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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Kältesofortkompresse — 2 UDI-DI variants, MDR (Gello GmbH Geltechnik)

MD Atlas
Gello GmbH Geltechnik

Data from EUDAMED, last updated May 23, 2026

Kältesofortkompresse

42517651AG50FA

2 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: Gello GmbH Geltechnik

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 42517651AG50FA
Device name: Kältesofortkompresse
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 28, 2024

Manufacturer & authorised representative

Manufacturer

Name: Gello GmbH Geltechnik
SRN: DE-MF-000010607
Country: Germany
Email: info@gello.de
Phone: +49256198020

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01HQQFDRKNJCQ9K7H7HEGB14G1

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

Instant cold pack04251765100290
Instant cold pack04251765100313