Eumedics Medizintechnik Und Marketing GmbH

Eumedics Medizintechnik Und Marketing GmbH holds 1 FDA 510(k) medical device clearance, cleared in 2009.

Top product codes for Eumedics Medizintechnik Und Marketing GmbH

BWF — Anesthesiology1 device

Recent clearances by Eumedics Medizintechnik Und Marketing GmbH

K080299 — RESPIFIT S, MODEL RS-LR1001004Code BWF·2009-01-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.