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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™ prestopor supermiękki — 7 UDI-DI variants, MDR

MD Atlas
3M Deutschland GmbH (Medical)

Data from EUDAMED, last updated May 23, 2026

Viscoplast™ prestopor supermiękki

06082232761050000000007GM

7 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: 06082232761050000000007GM
Device name: Viscoplast™ prestopor supermiękki
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class I
Version date: Apr 15, 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

7 UDI-DI variants

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Export results

Applied filters

basicUdiUlid01KP86FTVG5T3BCAG2EKXA7N7V

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

Nexcare™ Bandages soft touch universal04054596926769
Nexcare™ Bandages soft touch universal04064035096403
not applicable05902658312199
not applicable05902658312182
not applicable04064035061166
not applicable05902658312205
not applicable04064035061173