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EUDAMED last updated this device on Mar 14, 2024
B-05904365620192PL-MF-0000376425904365620MEH4On the marketAB Group Serum5904365620KOLBLOn the marketAnti-IgG reagentB-05904365620222On the marketCoated Standardized Red Blood Cells ORhD+ with anti-D antibodiesB-05904365620109On the marketCoated Standardized Red Blood Cells ORhD+ with anti-D antibodies READY TO USEB-05904365620116On 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.
(01)05904365620192
European Medical Device Nomenclature — the EU product classification assigned to this device.
W0103030304POLYSPECIFIC ANTIHUMAN SERUM