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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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Kältespray — 3 UDI-DI variants, MDR (Aerochemica Dr. Deppe GmbH)

MD Atlas
Aerochemica Dr. Deppe GmbH

Data from EUDAMED, last updated May 23, 2026

Kältespray

4028641AEK001BR

3 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: Aerochemica Dr. Deppe GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 4028641AEK001BR
Device name: Kältespray
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 25, 2024

Manufacturer & authorised representative

Manufacturer

Name: Aerochemica Dr. Deppe GmbH
SRN: DE-MF-000004990
Country: Germany
Email: info@aerochemica.de
Phone: +49 2152 80 97 100

Variants by status

UDI-DI variants

3 UDI-DI variants

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Applied filters

basicUdiUlid01J174H2A77Z73511XV7QQWTXJ

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

40313604028641000049
40313504028641000056
40318304028641000032