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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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PlasmaDerm Dress — 1 UDI-DI variant, MDR (CINOGY GmbH)

MD Atlas
CINOGY GmbH

Data from EUDAMED, last updated May 31, 2026

PlasmaDerm Dress

42606711700486

1 UDI-DI variant

MDR [Regulation (EU) 2017/745 on medical devices]Class IIa

Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Manufacturer: CINOGY GmbH

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Device characteristics

Active device

Identity & classification

Basic UDI-DI: 42606711700486
Device name: PlasmaDerm Dress
Issuing agency: GS1
Legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Risk class: Class IIa
Version date: May 27, 2026

Manufacturer & authorised representative

Manufacturer

Name: CINOGY GmbH
SRN: DE-MF-000048574
Country: Germany
Email: eudamed@cinogy.de
Phone: +495527746970

Variants by status

UDI-DI variants

1 UDI-DI variant

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Export results

Applied filters

basicUdiUlid01KSM59Y7Z1TDDK91YMJ2C4B5X

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

PlasmaDerm Dress04260671170037