- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on May 27, 2026
5400951PARSHAMPBCZJParanix Šampón + Pieptene is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class I. Manufactured by Omega Pharma International NV. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05400951005454CT321611 packaging level registered — each level carries its own UDI-DI.
05400951005454× 1 unitBase unit05400951004594× 2 units(01)05400951005454
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 eyes and mucous membranes. In case of contact with eyes or mucous membranes, rinse thoroughly with water. In case of irritation or allergic reaction, stop using the_product. If irritation persists, consult a doctor. Keep out of reach of children. Do not use on children under 2 years old. For external use only. In case of accidental ingestion, consult a doctor or the anti-poison centre. Make sure you washout the product well. Always respect the duration of the treatment. Do not use the product under occlusion, e.g. by covering up the hair with a cap or wrapped foil. If you accidentally spill the product, wash the floor thoroughly and immediately with soap and hot water to avoid the risk of slipping.
BE-PR-000007211The 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 →No certificate specifically references this device's Basic UDI-DI.
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.5400951PARLOTIONACTKOn the marketParanix Express Loção + Pente5400951PAREXPLOTIONCZ7On the marketParanix Express Lotion + Peigne5400951PAREXPLOTIONCZ7On the marketParanix Shampoing/Shampoo + Peigne/Kamm5400951PARTREATSHAMPC3TOn the marketParanix Spray + Ktena5400951PARLOTIONACTKOn the marketParanix Trattamento Shampoo + Pettine5400951PARTREATSHAMPC3TOn the market