9 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PORTABLE ELECTRIC MOTOR-HANDPIECE UNIT, HANDY-MATE
FDA 510(k)
FDA Class 1
·Dental
Procallus Fixator
FDA UDI
ORTHOFIX SRL·18032568863277·RADIOLUCENT ANKLE CLAMP KIT STERILE
3701 P37,SPECIAL LIGHT WIRING,STKR
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828100472·3701 P37,SPECIAL LIGHT WIRING,STKR
QT Scanner 2000 Model A
FDA 510(k)
FDA Class 2
·Radiology
CARDIOTECH SPIROMETRY SYSTEM, MODEL GT-105
FDA 510(k)
FDA Class 2
·Anesthesiology
PROSTHESIS, HIP, SEMI-CONSTRAINED, UNCEMENTED, METAL/POLYMER, NON-POROUS, CALICU
FDA Adverse Event
Injury
·SMITH & NEPHEW, INC.·Product code MEH·October 15, 2025
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·March 5, 2013
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Death
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011