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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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AIO22F.1 — 4 UDI-DI variants, MDR (Rein medical GmbH)

MD Atlas
Rein medical GmbH

Data from EUDAMED, last updated May 23, 2026

AIO22F.1

406163100000AIO22F1C7

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: 406163100000AIO22F1C7
Device name: AIO22F.1
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jul 22, 2024

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

basicUdiUlid01J3CZJ9KXPCZX8X5K0HFE8G7C

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

C722CF.204061631302099
C722CF.104061631300071
C722CFT.204061631302105
C722CFT.104061631300088