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EUDAMED last updated this device on Jun 2, 2025
59041832VIRGOSGPL-MF-00004028959041832AERON3On 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 marketNo 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.Primary placement in Poland; available across 1 country total.
Placed on the market in Poland; per-country availability dates not published.
European Medical Device Nomenclature — the EU product classification assigned to this device.
V0499CLINICAL USE CONTAINERS (NON-IVD) - OTHER