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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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Vevia Vankka Tripla — 2 UDI-DI variants, MDR (Vevia Finland Oy)

MD Atlas
Vevia Finland Oy

Data from EUDAMED, last updated May 23, 2026

Vevia Vankka Tripla

6429810258VTH2301NK

2 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: Vevia Finland Oy

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 6429810258VTH2301NK
Device name: Vevia Vankka Tripla
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 22, 2023

Manufacturer & authorised representative

Manufacturer

Name: Vevia Finland Oy
SRN: FI-MF-000006502
Country: Finland
Email: ville.aalto@vevia.fi
Phone: +358405547707

Variants by status

UDI-DI variants

2 UDI-DI variants

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Applied filters

basicUdiUlid01H11MYEVX65MW7YHKYRSVPDBR

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

Vevia Vankka Tripla06429810258502
Vevia Vankka Tripla06429810258519