24 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
SUPER 14
FDA 510(k)
FDA Class 2
·Dental
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040099605·Gutta Percha Points Cadm Free
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·H65810023021·Gutta Percha Points Cadm Free
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·10304040140519·Gutta Percha Points Cadm Free
SoftTip® large
FDA UDI
Honeywell Healthcare Solutions GmbH·04036616010245·SoftTip® large R-2203-16 AMC
OptiMesh 1500 S
FDA UDI
SPINEOLOGY INC.·M7403002302·Surgical Mesh
UNIVERSAL PLUS
FDA UDI
Conmed Corporation·30653405011518·UNIVERSAL PLUS, SUMP CANNULA WITH SIDE HOLES, S...
BR Surgical, LLC
FDA UDI
BR Surgical, LLC·00857556008260·Laparoscope, 4K, autoclavable, Ø 5.5mm, 0º, 302mm
ARTHROCARE SYSTEM 2000 CONTROLLER, ARTHROCARE SYSTEM 2000 CABLE, ARTHROCARE SYSTEM 2000 FOOTSWITCH, PLASMA SCALPEL GS, C
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HARDY DISK, PENICILLIN, 10 UNITS
FDA 510(k)
FDA Class 2
·Microbiology
PRIMUS HI
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SOLUTIONS USA, INC.·Product code IYE·March 13, 2013
ASR UNI FEMORAL IMPL SIZE 49
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD·Product code KWA·February 18, 2011
RAPAMYCIN CLINICAL 2.5 X 18MM
FDA Adverse Event
Injury
·CORDIS EUROPA, N.V.·Product code NIQ·February 22, 2008
ELEVATOR #301
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016
ELEVATOR #301
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016
ELEVATOR #301
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016
ELEVATOR #301
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016
ELEVATOR #301
FDA Adverse Event
Malfunction
·BIOMET MICROFIXATION·Product code EMJ·June 2, 2016
LORENZ 1.5 MM NEURO PACK/LORENZ 2.0 FT PLATES
FDA Adverse Event
Injury
·BIOMET MICROFIXATION·Product code JEY·May 27, 2015
AS LVP 20D 3SS CV
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FPA·September 28, 2020