11 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DEPUY DUPONT ORTHOPAEDICS FINGER JOINT PROSTHESIS
FDA 510(k)
FDA Class 2
·Orthopedic
artegral
FDA UDI
Merz Dental GmbH·D7091970544·anteriors; shade BL3; mould UBXL
Langston dual lumen catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
SCISSORS, BANDAGE, 15,18,20CM., ANGULAR
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
VARISOFT
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 12, 2024
VARISOFT
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·September 12, 2024
SEE H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL LIFECOR CORPORATION·Product code MVK·June 10, 2014
SEE H-10
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code HQL·February 20, 2013
MINICAP EXTEND LIFE PD TRANSFSET W/TWIST CLAMP
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·January 25, 2011
CERAMIC ELECTRODE TIP L-HK F/GK372R
FDA Adverse Event
Injury
·AESCULAP AG·Product code GEI·July 5, 2019