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EUDAMED last updated this device on May 22, 2026
5400951PARTREATSHAMPC3TParanit kezelő sampon + fésű is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Omega Pharma International NV. Placed on the EU market in Hungary. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05400951005287CT300311 packaging level registered — each level carries its own UDI-DI.
05400951005287× 2 unitsBase unit05400951003535× 2 units(01)05400951005287
European Medical Device Nomenclature — the EU product classification assigned to this device.
V901001LICE ELIMINATION MECHANICAL DEVICES1 warning recorded — scroll inside the panel to see all entries.
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). Serious incidents must be reported to Perrigo Belgium NV, Omega Pharma International NV, and the competent local authority.
Primary placement in Hungary; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| HungaryPrimary placement | — | Still on market |
BE-MF-000007210The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Sterile
A sterile device is supplied free of viable micro-organisms — flagged so that it is handled, stored and used to preserve that sterile state.
View in glossary →Single-use device
A single-use device is intended to be used on one patient during a single procedure and then discarded — not reprocessed or reused.
View in glossary →Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
View in glossary →CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
View in glossary →Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
View in glossary →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 →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 →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 →MDR risk classes
MDR risk classes rank medical devices from lowest risk (Class I) to highest (Class III), which determines how much regulatory scrutiny they face.
View in glossary →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 →5400951PARSHAMPBCZJOn the marketParanit Express Šampón + Hrebeň5400951PARSHAMPBCZJOn the marketParanit Express Шампоан + гребен5400951PARSHAMPBCZJOn the marketParanit Šampon + Glavnik5400951PARTREATSHAMPC3TOn the marketParanit Shampoo + Comb5400951PARTREATSHAMPC3TOn the marketParanit Sprej + Hřeben5400951PARLOTIONACTKOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate health across this manufacturer's portfolio.
20311GB448260506SupplementedNotified body
A notified body is an independent organisation, designated by an EU country, that audits manufacturers and certifies higher-risk devices before they can be CE-marked.
View in glossary →