40 results · 22ms · Sources: EU EUDAMED, US FDA

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Frax 1550 for Ellipse Nordlys/ Ellipse Nordlys+, Ellipse Sirius, Ellipse Infinity, Ellipse Mjolner, Ellipse Nordlys Ultra

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

SLIM ONEBODY SYSTEM

FDA 510(k)
FDA Class 2 ·Dental

BAR PEDICLE SCREW SPINAL FIXATION SYSTEM, MODEL 2020

FDA 510(k)
FDA Class 2 ·Orthopedic

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·February 22, 2022

T:SLIM X2 INSULIN PUMP WITH BASAL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code OZO·January 24, 2019

GEMINI PC1CE, 220V AUST

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

ONE TOUCH ULTRA

FDA Adverse Event
Malfunction ·LIFESCAN, INC.·Product code CFR·October 29, 2002

GEMINI PC1CE, 220V AUST

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·August 31, 2023

INFUSION PUMP/CONTROLLER

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

GEMINI PC1CE, 220V AUST

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

PC1 INTERNATIONAL ENGLISH

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

GEMINI PC1CE, 220V AUST

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

INFUSION PUMP/CONTROLLER

FDA Adverse Event
Malfunction ·ALARIS MEDICAL SYSTEMS·Product code FRN·April 19, 2001

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 27, 2023

PRIMEADVANCED

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·May 9, 2013

OT ULTRALINK METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

UNKNOWN CUP

FDA Adverse Event
Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code JDI·July 8, 2011

OT VERIO PRO METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 10, 2014

UNKNOWN IMPLANTABLE NEUROSTIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 10, 2015