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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

CT30030 — Class I MDR by Omega Pharma…

MD Atlas
Omega Pharma International NV

EUDAMED last updated this device on May 22, 2026

CT30030

5400951PARTREATSHAMPC3T

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Omega Pharma International NV
UDI-DI code: 05400951005096
Reference / catalog number: CT30030

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View device family (Basic UDI)

Manufacturer information

Organization name: Omega Pharma International NV
SRN: BE-MF-000007210
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
Avoid contact with the eyes and mucous membranes. In case of contact, rinse thoroughly with water. If eye irritation persists, consult a doctor. Do not swallow. If the product is accidentally swallowed, contact a doctor or poison control centre. Do not use on irritated skin. Do not use if you are allergic to perfume or to any of the listed ingredients. If skin rash, irritation, or sensitivity occurs, stop treatment immediately and wash hair with regular shampoo. Keep out of reach of children. For external use only. This product is exclusively intended for the treatment of head lice (not body lice or pubic lice).

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Market distribution

Primary placement in EL; available across 2 countries total.

Country	On market since	Until
ELPrimary placement		Still on market
Cyprus		Still on market

Device identification

Trade name: not provided
UDI-DI code: 05400951005096
Basic UDI-DI: 5400951PARTREATSHAMPC3T
Reference / catalog number: CT30030
Issuing entity: GS1

Classification

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

Device details

Quantity: 2
Additional product description: PARANIX Treatment Shampoo 200ml+comb GR
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

EMDN nomenclature code(s)

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

V901001LICE ELIMINATION MECHANICAL DEVICES

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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