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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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KomfiTilt — 3 UDI-DI variants, MDR (Vikta ApS)

MD Atlas
Vikta ApS

Data from EUDAMED, last updated May 31, 2026

KomfiTilt

57450011420083

3 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: Vikta ApS

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 57450011420083
Device name: KomfiTilt
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Mar 19, 2025

Manufacturer & authorised representative

Manufacturer

Name: Vikta ApS
SRN: DK-MF-000044091
Country: Denmark
Email: info@vikta.dk

Variants by status

UDI-DI variants

3 UDI-DI variants

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basicUdiUlid01JPQEXVZZ17NR95S19T47852Z

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

KomfiTilt ED.3 lateral tilt System05745001142476
KomfiTilt ED.5 lateral tilt05745001142001
KomfiTilt Go lateral tilt System05745001142490