168 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CARDIOVASCULAR TEMP. PACEMAKER ELEC
FDA 510(k)
FDA Class 2
·Cardiovascular
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117728·Modular Tibia Tray Trial Size 3
LEONE SPA
FDA UDI
LEONE SPA·08033707027195·WEB 1ST MOLAR BANDS n.UR 3
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88200031·Max. 1. Molar band W-Fit left 03
LeadCare® Plus Data ManagementSystem
FDA UDI
MAGELLAN DIAGNOSTICS, INC.·00850355006116·LeadCare® Plus Data ManagementSystem
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88200030051·Max. 1. Molar band W-Fit left 03
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88200030501·Max. 1. Molar band W-Fit left 03
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR88200030101·Max. 1. Molar band W-Fit left 03
ELECTROCARDIOGRAPH (ECG) ELECTRODE, NON-STERILE
FDA 510(k)
FDA Class 2
·Cardiovascular
NUCAL
FDA 510(k)
FDA Class 2
·Dental
STARDRIVE SCREWDRIVER SHAFT T4/66MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code HXX·May 20, 2014
MECHANICAL WALKER, ROLLATOR
FDA Adverse Event
UNKNOWN·Product code ITJ·November 5, 2012
ON-Q PAINBUSTER
FDA Adverse Event
Other
·I-FLOW CORP.·Product code MEB·August 25, 2010
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VERSATRAX MODEL 7000 UNIVERSAL A-V PULSE GENERATOR
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 9, 2016
ADAPTA DR
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
ADAPTA D
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·June 10, 2015
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, PLC·Product code DXY·March 27, 2015
PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code DXY·June 9, 2015
PULSE GENERATOR, PERMANENT, IMPLANTABLE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code NVZ·March 27, 2015