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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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Viscoplast ™ Zestaw Uniwersalny — 5 UDI-DI variants, MDR

MD Atlas
3M Deutschland GmbH (Medical)

Data from EUDAMED, last updated May 23, 2026

Viscoplast ™ Zestaw Uniwersalny

06082232761050000000008GP

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: 3M Deutschland GmbH (Medical)

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Device characteristics

No device characteristics flagged

Identity & classification

Basic UDI-DI: 06082232761050000000008GP
Device name: Viscoplast ™ Zestaw Uniwersalny
Device model: V12M3Z24
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: May 7, 2026

Manufacturer & authorised representative

Manufacturer

Name: 3M Deutschland GmbH (Medical)
SRN: DE-MF-000011641
Country: Germany
Email: Info-Medical-EU@solventum.com

Variants by status

UDI-DI variants

5 UDI-DI variants

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Applied filters

basicUdiUlid01KR13C4Q056398XK656GW9Y2Y

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

V12M3Z2404054596798328
V0-22-06-S04064035157708
V0-26-5TP04064035157678
V0-22-5T04064035146368
V12M1Z1704054596798342