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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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Dental Scanbodies — 13 UDI-DI variants, MDR

MD Atlas
GMI Dental Implantology, S.L.

Data from EUDAMED, last updated May 23, 2026

Dental Scanbodies

843656274KDI00E2

13 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: GMI Dental Implantology, S.L.

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 843656274KDI00E2
Device name: Dental Scanbodies
Device model: 843656274KDI00E2
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2026

Manufacturer & authorised representative

Manufacturer

Name: GMI Dental Implantology, S.L.
SRN: ES-MF-000024246
Country: Spain
Email: info@gmidental.com
Phone: +34 973 18 43 50

Variants by status

UDI-DI variants

13 UDI-DI variants

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Applied filters

basicUdiUlid01KS7VS6ERM56QEBFSKT0JXY7T

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

KDI0F000208436562745882
KDI0F400408436562745820
KDI0F400608436562748746
KDI0F360208436562745110
KDI0F400208436562742027
KDI0F000308436562745837
KDI0F360108436562745103
KDI0F400508436562748760
KDI0F360408436562745806
KDI0F400108436562742010
KDI0F360308436562745790
KDI0C400308436562742034
KDI0F000408436562746766