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EUDAMED last updated this device on Jun 23, 2026
B-08595566424695Plastry na odciski z kwasem salicylowym is an MDD-legacy 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.
PL-MF-000010968TNP/MDD/0322/3906/2020(01)08595566424695
4 warnings recorded — scroll inside the panel to see all entries.
w przypadku wątpliwości lub wystąpienia objawów niepożądanych należy skonsultować się lekarzem
Użycie wyrobu niezgodnie z jego przewidzianym zastosowaniem (w tym powtórne) grozi uszkodzeniem ciała lub nieskutecznością usunięcia odcisku
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
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 1 country total.
| Country | On market since | Until |
|---|---|---|
| CzechiaPrimary placement | Sep 17, 2020 | Still on market |
Primary DI
The Primary DI is the main UDI-DI a manufacturer designates as the principal identifier for a device in EUDAMED.
08595566424695Basic UDI-DI
The Basic UDI-DI is the main identifier that groups together all device variants of the same model — the regulatory "family" key.
B-0859556642469512-24695UDI issuing entities
Issuing entities are the organisations the European Commission has designated to assign Unique Device Identifiers under the EU's UDI system.
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.
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 →B-05901448250611On the marketPlastry na odciski z kwasem salicylowym590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowym590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowym komfortB-05903856882736On the marketPlastry na odciski z kwasem salicylowym komfort590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowym plus590144825CORNPLASTERDNOn the marketNo certificate specifically references this device's Basic UDI-DI.
Certificate 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 →