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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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Vela Meywalk — 9 UDI-DI variants, MDR (Vermund Larsen A/S)

MD Atlas
Vermund Larsen A/S

Data from EUDAMED, last updated May 23, 2026

Vela Meywalk

57143390009PY

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: Vermund Larsen A/S

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 57143390009PY
Device name: Vela Meywalk
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 12, 2026

Manufacturer & authorised representative

Manufacturer

Name: Vermund Larsen A/S
SRN: DK-MF-000002203
Country: Denmark
Email: mail@vela.dk

Variants by status

UDI-DI variants

9 UDI-DI variants

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Applied filters

basicUdiUlid01KRDSESRK17G0KKK2FT15FCZW

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

Vela Meywalk 200 Small05714339918282
Vela Meywalk 2000 Large05714339918268
Vela Meywalk 2000 Medium05714339918275
Vela Meywalk 4 Medium05714339918169
Vela Meywalk 4 Micro05714339918251
Vela Meywalk 4 Small05714339918244
Vela Meywalk Large05714339918237
Vela Miniwalk size 105714339918299
Vela Miniwalk size 205714339918305