EUDAMED last updated this device on May 20, 2026

Paranix Express Loção + Pente

5400951PAREXPLOTIONCZ7

On the marketClass I

Applicable legislation: —
Organization name: Omega Pharma International NV
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 →: 05400951005072
Reference / catalog number: CT32080

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.

Paranix Express Loção + Pente is an EU-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Omega Pharma International NV. Placed on the EU market in Portugal. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.

Device identification

Trade name: Paranix Express Loção + Pente
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 →: 05400951005072
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 →: 5400951PAREXPLOTIONCZ7
Reference / catalog number: CT32080
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: 2
Additional product description: PARANIX Express lotion 95ml+comb PT
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

Packaging levels

1 packaging level registered — each level carries its own UDI-DI.

05400951005072× 2 unitsBase unit
- 05400951004761× 2 units

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

UDI-DI DataMatrix

Encoded

(01)05400951005072

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.

V901001LICE ELIMINATION MECHANICAL DEVICES

Critical warnings

No critical warnings reported for this device.

Compliance flags

Safety

Direct marking

Regulatory

Sterilization

Lifecycle

New device

Market distribution

Primary placement in Portugal; available across 1 country total.

Country	On market since	Until
PortugalPrimary placement	Jan 1, 2000	Still on market

Paranix Express Loção + Pente

Device identification

Classification

Device details

Packaging levels

UDI-PI traceability

UDI-DI DataMatrix

UDI-PI DataMatrix

EMDN nomenclature code(s)

Critical warnings

Compliance flags

Safety

Regulatory

Lifecycle

Market distribution

Related searches

Device identification

Classification

Device details

Packaging levels

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 covering this device

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Certificates