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EUDAMED last updated this device on May 22, 2026
5410765SolverRTNALOX EASY is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class IIa. Manufactured by Oystershell NV. Placed on the EU market in Finland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
0541076500976007011760(01)05410765009760
European Medical Device Nomenclature — the EU product classification assigned to this device.
M0410DRESSINGS FOR NAILS IN THE FORM OF LIQUIDS, GELS AND CREAMS10 warnings recorded — scroll inside the panel to see all entries.
OTHER
Keep out of reach of children
Do not use past indicated date
Primary placement in Finland; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| FinlandPrimary placement | — | Still on market |
| Sweden | — | Still on market |
BE-MF-000011797The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
Causes serious eye damage
IF IN EYES Rinse cautiously with water for several minutes.
Keep container tightly closed
Causes skin irritation
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 →5410765SilcapShampooG5On the marketMOSQUITO MED SHAMPOO 100ML5410765SilcapShampooG5On the marketNALOX EASY5410765SolverRTOn the marketOWIX HAIR S.O.S SZAMPON5410765ElimaxShampooCKOn the marketPLASTIC COMB BLUE NO LOGO WITH UDI5410765PlasticlicecombLVOn the marketPRIODERM ANTI-LUIS SHAMPOO 100ML5410765ElimaxShampooCKOn the marketNo 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.