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

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Wrist 3

FDA 510(k)
FDA Class 2 ·Radiology

HAMILTON-C6

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 8, 2024

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197058995·Nelaton grooved director 16 cm,...

Signature Cement Plug

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215008239·

Cement Plug

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215053741·

HAMILTON MEDICAL AG

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·April 5, 2023

OrthoMedFlex

FDA UDI
ORTHOMEDFLEX LLC·M7161111601850·Cement Plug, Size 21mm, LLDPE

NITRILE POWDER FREE PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

SLEEP APP

FDA 510(k)
FDA Class 2 ·Dental

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·July 29, 2022

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 17, 2022

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·September 10, 2020

IN00087 CLERMONT FERRAND PH

FDA Adverse Event
Death ·SORIN GROUP ITALIA·Product code DWF·March 7, 2014

STOCKERT 70 RF GENERATOR

FDA Adverse Event
Injury ·STOCKERT GMBH·Product code DRF·June 10, 2013

HS III PROXIMAL SEAL SYSTEM 3.8MM

FDA Adverse Event
Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·June 2, 2011

COLLEAGUE CX VOLUMETRIC INFUSION PUMP

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·September 16, 2008

INSPIRE 6F HOLLOW FIBER OXYGENATOR WITH INTEGRATED ARTERIAL FILTER AND HARDSHELL

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA·Product code DTZ·January 7, 2016

TRUETRACK

FDA Adverse Event
Malfunction ·TRIVIDIA HEALTH, INC.·Product code NBW·September 20, 2017

GMK-SPHERE FEMORAL COMPONENT CEMENTED SIZE 6 L

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·November 11, 2020

INSPIRE 6F HOLLOW FIBER OXYGENATOR

FDA Adverse Event
Malfunction ·SORIN GROUP ITALIA SRL·Product code DTZ·April 21, 2022