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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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Abutment — 5 UDI-DI variants, MDR (Medical Consult Implants GmbH)

MD Atlas
Medical Consult Implants GmbH

Data from EUDAMED, last updated May 23, 2026

Abutment

426055181Scan-PostKS

5 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: Medical Consult Implants GmbH

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 426055181Scan-PostKS
Device name: Abutment
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Jun 9, 2022

Manufacturer & authorised representative

Manufacturer

Name: Medical Consult Implants GmbH
SRN: DE-MF-000019273
Country: Germany
Email: kundeninfo@mci-implants.de
Phone: 02841882710

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01G54H0BWD6TN6G3ZE64WGGTY0

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

Scanbody for Ø 3,75 Cercon04260551815706
Scanbody Ø 3,304260551810923
Scanbody Ø 3,8/4,104260551813023
Scanbody Ø 4,504260551811869
Scanbody Ø 5,504260551812477