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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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Scan Body — 4 UDI-DI variants, MDR (MEDIGMA BIOMEDICAL GMBH)

MD Atlas
MEDIGMA BIOMEDICAL GMBH

Data from EUDAMED, last updated May 23, 2026

Scan Body

426073577ScanBodyBT

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: MEDIGMA BIOMEDICAL GMBH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426073577ScanBodyBT
Device name: —
Device model: Scan Body
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 13, 2024

Manufacturer & authorised representative

Manufacturer

Name: MEDIGMA BIOMEDICAL GMBH
SRN: DE-MF-000009412
Country: Germany
Email: office@medigma-implants.com

Variants by status

UDI-DI variants

4 UDI-DI variants

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Applied filters

basicUdiUlid01HPGZ55SFC2XTFH7F8E727DF9

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

Grand Konisch™ Scan Body 10mm04260735770203
Grand Konisch™ Scan Body 7mm04260735770197
Single Unit Scan Body 6mm04260735774263
Single Unit Scan Body 9mm04260735774287