EUDAMED last updated this device on Aug 7, 2026

ViroCAP med Spacer

426251894-VC_Spacer_s-U5

On the marketClass I

Applicable legislation: —
Organization name: Viromed Medical AG
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04262518941534
Reference / catalog number: 153

Regulatory classification unavailableThis product's Basic UDI record hasn't been published in EUDAMED yet. Classification and compliance details will appear automatically once EUDAMED publishes it.

ViroCAP med Spacer is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Viromed Medical AG. Placed on the EU market in Germany. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: ViroCAP med Spacer
Primary DI The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED. View in glossary →: 04262518941534
Basic UDI-DI The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key. View in glossary →: 426251894-VC_Spacer_s-U5
Reference / catalog number: 153
UDI issuing entities Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system. View in glossary →: GS1

Classification

Risk category: Class I
Applicable legislation: —
Status: On the market

Device details

Quantity: 12
Additional product description: Der Spacer ist ein steriler Einwegartikel, der in die Vorderseite des Gehäuses des mobilen Geräts eingesetzt wird, um einen sicheren Abstand zwischen dem Plasmamodul und dem zu behandelnden Bereich zu gewährleisten. Der Spacer darf nur für eine einzige Behandlung (z. B. einer Wunde) pro Patient verwendet werden, um eine Kreuzkontamination durch verschiedene Wunden zu verhindern. Der Spacer schützt außerdem den Benutzer, indem er durch ein Schutzgitter den Kontakt mit der Plasmaquelle verhindert.
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)04262518941534

UDI-PI DataMatrix

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

EMDN nomenclature code(s)

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

Z12019003WOUND TREATMENT EQUIPMENT

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Certificates covering this device

No certificate specifically references this device's Basic UDI-DI.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jul 6, 2026	Still on market

ViroCAP med Spacer

Device identification

Classification

Device details

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates covering this device

Market distribution

Related searches

Device identification

Classification

Device details

Manufacturer information

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Certificates

Certificates covering this device

Related devices

Market distribution

Related searches

Manufacturer information

Certificates

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