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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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Magnus 22 — 4 UDI-DI variants, IVDR (Álvarez Redondo, S.A.)

MD Atlas
Álvarez Redondo, S.A.

Data from EUDAMED, last updated May 23, 2026

Magnus 22

843661198-IVD-MGN2-FL

4 UDI-DI variants

IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]IVDR Class A

Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Manufacturer: Álvarez Redondo, S.A.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843661198-IVD-MGN2-FL
Device name: Magnus 22
Device model: CE 230IVD
Issuing agency: GS1
Legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk class: IVDR Class A
Version date: Dec 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: Álvarez Redondo, S.A.
SRN: ES-MF-000000560
Country: Spain
Email: info@ortoalresa.com
Phone: +34 91 884 40 16

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01JER7B7MAHN464K88ZH6VPRGV

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

CE 230IVD08436611980677
CE 231IVD08436611980684
CE 237IVD08436611980738
CE 236IVD08436611980721