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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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The AIO Solution® (All-in-One Patient… — 6 UDI-DI variants, MDR

MD Atlas
Orfit Industries

Data from EUDAMED, last updated May 23, 2026

The AIO Solution® (All-in-One Patient Positioning Solution)

5420028700304T

6 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: Orfit Industries

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5420028700304T
Device name: The AIO Solution® (All-in-One Patient Positioning Solution)
Device model: 0030
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jan 30, 2025

Manufacturer & authorised representative

Manufacturer

Name: Orfit Industries
SRN: BE-MF-000007872
Country: Belgium
Email: welcome@orfit.com
Phone: +32 3 326 20 26

Variants by status

UDI-DI variants

6 UDI-DI variants

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Applied filters

basicUdiUlid01JJ6W650G2GEHWWMRZAAPZW0J

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

3824654011720037055
3824754011720037338
The AIO Solution® (All-in-One Patient Positioning Solution)54011720037482
The AIO Solution® (All-in-One Patient Positioning Solution)54011720036966
The AIO Solution® (All-in-One Patient Positioning Solution)05420028702833
The AIO Solution® (All-in-One Patient Positioning Solution)54011720036973