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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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AIOS22F.0 — 4 UDI-DI variants, MDR (Rein medical GmbH)

MD Atlas
Rein medical GmbH

Data from EUDAMED, last updated May 23, 2026

AIOS22F.0

406163100000AIOS22F0V9

4 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: Rein medical GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 406163100000AIOS22F0V9
Device name: AIOS22F.0
Device model: All-in-One Computer
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 6, 2022

Manufacturer & authorised representative

Manufacturer

Name: Rein medical GmbH
SRN: DE-MF-000018721
Country: Germany
Email: info@reinmedical.com
Phone: +49216169840

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01FZFX31Y0JSYBY5QDM44PG4AK

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

CS522TCF.104061631300569
CS522CF.104061631300545
CS522CFT.104061631300552
CS522TCFT.104061631300576