24 results · 25ms · Sources: EU EUDAMED, US FDA

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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