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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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coolPack mini — 2 UDI-DI variants, MDR (Coolike Regnery GmbH)

MD Atlas
Coolike Regnery GmbH

Data from EUDAMED, last updated May 23, 2026

coolPack mini

4010054R33424WC

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: Coolike Regnery GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4010054R33424WC
Device name: coolPack mini
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 3, 2022

Manufacturer & authorised representative

Manufacturer

Name: Coolike Regnery GmbH
SRN: DE-MF-000017788
Country: Germany
Email: info@coolike.de
Phone: +49 6251 8450 0

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01G4M8PP5AWTK968JQ2TSE63XE

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

6145 01000, 6145 08000, 6145 0101204010054009290
6093 01000, 6095 01000, 6173 08000, 6225 08000, 6100 08000, 6094 08000, 6115 0100004010054009276