40 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: 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