9 results
·
23ms
·
Sources: EU EUDAMED, US FDA
P.F.C. CEMENT PRESSURIZING SYSTEM
FDA 510(k)
FDA Class 1
·Orthopedic
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471193444·K-WIRE - SINGLE TROCAR 3.0mm DIA x 150mm
S5362 REF 943-906
FDA UDI
Radiometer Medical ApS·05700699439062·S5362 Hypochlorit Solution for protein Removal ...
SNYDER HEMOVAC WOUND DRAINAGE DEVICES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
PERCUTANEOUS CATHETER INTRODUCER KIT
FDA 510(k)
FDA Class 2
·Cardiovascular
REDUC-FORC W/POINT SOFTLO L155
FDA Adverse Event
Malfunction
·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code HTD·March 19, 2019
PINN MAR +4 NEUT 32IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·February 5, 2013
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LKK·December 28, 2010
COBE SPECTRA BLOOD COLLECTION
FDA Adverse Event
Injury
·TERUMO BCT·Product code GKT·July 18, 2014