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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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CryoCE AC L2 — 81 UDI-DI variants, MDR

MD Atlas
Auguste Cryogenics Germany GmbH

Data from EUDAMED, last updated May 23, 2026

CryoCE AC L2

426241677MedicalFamilyCL

81 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: Auguste Cryogenics Germany GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426241677MedicalFamilyCL
Device name: CryoCE AC L2
Device model: Medical Family
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Mar 6, 2023

Manufacturer & authorised representative

Manufacturer

Name: Auguste Cryogenics Germany GmbH
SRN: DE-MF-000019115
Country: Germany
Email: cs.de@augustecryogenics.com
Phone: +49 4841 985120

Variants by status

UDI-DI variants

81 UDI-DI variants

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Applied filters

basicUdiUlid01GTV48M8EQANQ8YJT3V3HCKVP

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

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H-AAD210039304262416770748
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H-AAD210029404262416770526
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H-AAD210029604262416770588
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H-AAD210007404262416770267
H-AAD210007804262416770298
H-AAD210008404262416770311
H-AAD210010204262416770540

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