- Organization name
- UDI-DI code
- Reference / catalog number
EUDAMED last updated this device on Jun 24, 2026
590144825CORNPLASTERDNSPOFAPLAST náplasti na kuří oka s kyselinou salicylovou is an EU MDR-regulated medical device registered in EUDAMED. It is classified as Class III. Manufactured by LANGSTEINER SPÓŁKA Z OGRANICZONĄ ODPOWIEDZIALNOŚCIĄ. Placed on the EU market in Czechia. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05901448250826183PL-MF-000010968TNP/MDR/0057/3906/2026TNP/MDR/0058/3906/2026(01)05901448250826
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
4 warnings recorded — scroll inside the panel to see all entries.
w przypadku wątpliwości lub wystąpienia objawów niepożądanych należy skonsultować się lekarzem
substancje lecznicze działające pomocniczo: kwas salicylowy 35% i kwas mlekowy 1,2%; w przypadku znanej nadwrażliwości na kwas salicylowy, salicylany i na każdy z innych składników plastra; kwas salicylowy może zwiększać przepuszczalność skóry dla innych leków stosowanych lokalnie
użycie wyrobu niezgodnie z jego przewidzianym zastosowaniem (w tym powtórne) grozi uszkodzeniem ciała lub nieskutecznością usunięcia odcisku
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.
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.
Contains latex
A "contains latex" flag warns that a device contains natural rubber latex, which can trigger allergic reactions in sensitive patients.
CMR substance
A CMR flag warns that a device contains a substance that is carcinogenic, mutagenic or toxic to reproduction above a defined threshold.
Endocrine-disrupting substance
An endocrine-disruptor flag warns that a device contains a substance with endocrine-disrupting properties above a defined threshold.
Primary placement in Czechia; available across 2 countries total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Oct 1, 2019 | Still on market |
| Slovakia | Oct 1, 2019 | Still on market |
European Medical Device Nomenclature — the EU product classification assigned to this device.
M0412DRESSINGS FOR THE TREATMENT OF WARTS, CORNS AND CALLUSESPrimary 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 →590144825CORNPLASTERDNOn the marketSerum na grzybice paznokci590144825FUNGALNAILA8On the marketSPOFAPLAST náplasti na kuří oka s kyselinou salicylovouB-05901448250826On the marketTrekpleister Likdoorn verwijderpleisters met salicylzuur590144825CORNPLASTERDNOn the marketViscoplast plastry na odciski z kwasem salicylowym590144825CORNPLASTERDNOn the marketViscoplast Plastry na odciski z kwasem salicylowymB-05901448250796On the marketCertificate health across this manufacturer's portfolio.
TNP/MDR/0057/3906/2026IssuedTNP/MDR/0058/3906/2026IssuedNotified 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 →Notified 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 →