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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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Organization name
UDI-DI code
Reference / catalog number

PlasmaDerm Vario, Model… — Class IIa MDR by CINOGY GmbH

MD Atlas
CINOGY GmbH

EUDAMED last updated this device on May 27, 2026

PlasmaDerm Vario, Model PlasmaDerm Flex

4260671170017Y

On the marketClass IIa

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: CINOGY GmbH
UDI-DI code: 04260671170006
Reference / catalog number: K25200

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View device family (Basic UDI)

Manufacturer information

Organization name: CINOGY GmbH
SRN: DE-MF-000048574
Manufacturer status: Active

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW010
EUDAMED did not publish a description for this code.
CW014
EUDAMED did not publish a description for this code.
CW133
EUDAMED did not publish a description for this code.
CW273
EUDAMED did not publish a description for this code.

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Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: PlasmaDerm Vario, Model PlasmaDerm Flex
UDI-DI code: 04260671170006
Basic UDI-DI: 4260671170017Y
Reference / catalog number: K25200
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)04260671170006

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UDI-PI DataMatrix

The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.

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EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

Z12019003WOUND TREATMENT EQUIPMENT

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

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Related devices

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Certificates

Certificate health across this manufacturer's portfolio.

CR-03-1211-881-25Issued
Quality management systemNotified body: 0537Expiry: Aug 14, 2030