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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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Medical Freezer — 5 UDI-DI variants, MDR

MD Atlas
Auguste Cryogenics Slovakia s.r.o.

Data from EUDAMED, last updated May 31, 2026

Medical Freezer

8588009681ACFSDC

5 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 Slovakia s.r.o.

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Device characteristics

No device characteristics flagged

Legacy certificates

Certificate number: 2026-MDR/QS-012
Type: refdata.certificate-mdr-type.quality-management-system
Notified body: 3EC International a.s. (2265)
Validity: Feb 9, 2026 → Feb 9, 2031

Identity & classification

Basic UDI-DI: 8588009681ACFSDC
Device name: Medical Freezer
Device model: AC Medical Freezer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Feb 24, 2026

Manufacturer & authorised representative

Manufacturer

Name: Auguste Cryogenics Slovakia s.r.o.
SRN: SK-MF-000026173
Country: Slovakia
Email: cs.eu@augustecryogenics.com
Phone: +421 55 727 7124

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KJ81AVJR813KN3T0WGD43KGK

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

AC BIO 86008588009681021
AC SYS 48008588009681038
AC IVF 43008588009681014
AC BIO 430X08588009681045
AC BIO 43008588009681007