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EUDAMED last updated this device on Jun 25, 2026
B-05901448250611Plastry 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 Poland. Explore certificates, regulatory status and the EUDAMED record on MD Atlas.
05901448250611REF 40-0006 02(01)05901448250611
European Medical Device Nomenclature — the EU product classification assigned to this device.
M0412DRESSINGS FOR THE TREATMENT OF WARTS, CORNS AND CALLUSES3 warnings recorded — scroll inside the panel to see all entries.
CW009CW010CW264PL-MF-000010968TNP/MDD/0322/3906/2020Primary placement in Poland; available across 1 country total.
| Country | On market since | Until |
|---|---|---|
| PolandPrimary placement | Dec 14, 2015 | Still on market |
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.
590144825CORNPLASTERDNOn the marketLikdoorn verwijderpleisters met Salicylzuur590144825CORNPLASTERDNOn the marketLikdoorn verwijderpleisters met Salicylzuur590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowym590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowym590144825CORNPLASTERDNOn the marketPlastry na odciski z kwasem salicylowymB-08595566424695On 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 →