- Role
- Country
- Date of registration
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EUDAMED last updated this device on Jun 24, 2025
59041832CCAREGD0590418321798759041832CCAREGDMAT/CC1/87x200x10/REH/S(01)05904183217987
The compliance carrier: encodes the device identifier plus the production identifiers (lot, serial, dates) registered for this device.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V080702NON ACTIVE ANTI-DECUBITUS MEDICAL MATTRESSESNo certificate specifically references this device's Basic UDI-DI.
Primary placement in Poland; available across 1 country total.
Placed on the market in Poland; per-country availability dates not published.
PL-MF-000040289No 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.59041832AERON3On the marketASTER RECLINER ELECTRIC CADET ZEST 110 PACIFIC59041832ASTERELSWOn the marketASTER RECLINER ELECTRIC CADET ZEST 124 ELECTRIC BLUE59041832ASTERELSWOn the marketASTER RECLINER ELECTRIC CADET ZEST 201 JADE59041832ASTERELSWOn the marketASTER RECLINER ELECTRIC CADET ZEST 219 SEAFOAM59041832ASTERELSWOn the market