22 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OLYMPUS RF LATEX CALIBRATOR, AND OLYMPUS RF LATEX REAGENT WITH MODEL(S): ODC0028, AND OSR61105.
FDA 510(k)
FDA Class 2
·Immunology
“Paonan” Orthopedic Manual Surgical Instrument (Non-Sterile)
FDA UDI
Paonan Biotech Co.,Ltd.·04719878786881·Awl with Depth Stop
Mini-Mono®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70602011·Mini-Mono-Brackets Roth 'N' .022" 100 Brackets
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0600010·Tray Insert, Level 1
Ocata Anterior Cervical System
FDA UDI
Kalitec Direct LLC·B07308K0600010·Tray Insert 1, Ocata
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·January 31, 2007
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0602000·Tray base, 2"
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·February 16, 2007
BAYER ADVIA IMS SYSTEM
FDA 510(k)
FDA Class 2
·Clinical Chemistry
HARDYDISK, STREPTOMYCIN 10MCG
FDA 510(k)
FDA Class 2
·Microbiology
LAP DISC HAND ACCESS DEVICE
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·August 21, 2006
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code GIS·January 9, 2007
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·January 26, 2007
HOURGLASS
FDA Adverse Event
Injury
·MEDTRONIC·Product code MQP·June 16, 2014
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·October 20, 2006
PINN.SECTOR ACET.CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS·Product code KWA·April 16, 2013
ENDURANT II EXTENSION CUFF
FDA Adverse Event
Injury
·MEDTRONIC IREALAND·Product code MIH·September 4, 2014
STARCLOSE SE VASCULAR CLOSURE SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·April 15, 2011
ALTO
FDA Adverse Event
Injury
·ELA MEDICAL, S.A.S.·Product code MRM·February 1, 2006
CONFIDA BRECKER CURVE GUIDEWIRE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code DQX·June 5, 2025