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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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automated cryogenic lines for… — 1 UDI-DI variant, MDR (SOL S.p.A.)

MD Atlas
SOL S.p.A.

Data from EUDAMED, last updated May 30, 2026

automated cryogenic lines for cryobiological rooms

805934048CRYOBANKAZ

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: SOL S.p.A.

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 805934048CRYOBANKAZ
Device name: automated cryogenic lines for cryobiological rooms
Device model: automated cryogenic lines for cryobiological rooms
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: Oct 14, 2021

Manufacturer & authorised representative

Manufacturer

Name: SOL S.p.A.
SRN: IT-MF-000011280
Country: Italy
Email: materiovigilance@sol.it

Variants by status

UDI-DI variants

1 UDI-DI variant

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Applied filters

basicUdiUlid01FHFFCE6C197DJ1RSPB4APHC8

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

cryobank08059340480159