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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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Scanbody — 4 UDI-DI variants, MDR (OrangeCAD Med GmbH)

MD Atlas
OrangeCAD Med GmbH

Data from EUDAMED, last updated May 23, 2026

Scanbody

426236519193114215425RC

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: OrangeCAD Med GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426236519193114215425RC
Device name: Scanbody
Device model: Scanbody
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 2, 2026

Manufacturer & authorised representative

Manufacturer

Name: OrangeCAD Med GmbH
SRN: DE-MF-000023347
Country: Germany
Email: info@orangecad-med.com
Phone: +49 721 986188 - 00

Variants by status

UDI-DI variants

4 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KN6HCP2Y3MQT9AYJ3TX6QTQA

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

SMBL1901H04262365195722
SMBL1902H04262365195715
SMTL1902H04262365196217
SMTL1903H04262365196224