Getsch+Hiller Medizintechnik GmbH

Getsch+Hiller Medizintechnik GmbH holds 1 FDA 510(k) medical device clearance, cleared in 2017.

Top product codes for Getsch+Hiller Medizintechnik GmbH

GEI — General, Plastic Surgery1 device

Recent clearances by Getsch+Hiller Medizintechnik GmbH

K171523 — Monopolar Single Use Laparoscopic InstrumentCode GEI·2017-08-22

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