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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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Multi Small — 9 UDI-DI variants, MDR (Levabo ApS)

MD Atlas
Levabo ApS

Data from EUDAMED, last updated May 23, 2026

Multi Small

5711014ALLUPPM

9 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: Levabo ApS

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 5711014ALLUPPM
Device name: Multi Small
Device model: All Up
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Feb 10, 2024

Manufacturer & authorised representative

Manufacturer

Name: Levabo ApS
SRN: DK-MF-000014646
Country: Denmark
Email: ke@levabo.dk
Phone: +4540220333

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01HP94GDRTDQNEDVYTQKKVV41E

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

8008005711014800801
7614005711014761409
8021305711014802133
8001105711014800115
7601405711014760143
7000405711014700040
8000305711014800030
8001005711014800108
8000605711014800061