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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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Avalon vinyylikäsine / Avalon vinyl… — 5 UDI-DI variants, MDR

MD Atlas
Walki Medical Oy

Data from EUDAMED, last updated May 23, 2026

Avalon vinyylikäsine / Avalon vinyl glove

643847971WM2Q

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: Walki Medical Oy

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UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01GF64S19BT5AJYBT81K63ENDZ

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

713006438479713055
712006438479712058
711006438479711051
714006438479714052
710006438479710054

Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 643847971WM2Q
Device name: Avalon vinyylikäsine / Avalon vinyl glove
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Oct 13, 2022

Manufacturer & authorised representative

Manufacturer

Name: Walki Medical Oy
SRN: FI-MF-000006903
Country: Finland
Email: myynti@walkimedical.fi

Variants by status