35 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DOPPLEX CENTRALE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
Mini-Mono® Brackets
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70602301·Mini-Mono-Brackets Andrews 'N' .018" 100 Brackets
UNIVERSAL F2®
FDA UDI
King Systems Corporation·00612649200071·UNIVERSAL F2 CIRCUIT
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K0602000·Tray base, 2"
TRIAGE B-TYPE NATRIURETIC PEPTIDE (BNP) CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
DIASOL-BICARB
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
SELOX SR 45
FDA Adverse Event
Injury
·BIOTRONIK GMBH AND CO.·Product code DTB·November 3, 2006
SELOX ST 53
FDA Adverse Event
Injury
·BIOTRONIK GMBH CO.·Product code DTB·November 3, 2006
Widex
FDA UDI
Widex A/S·05706069673340·Widex EVOKE E-CIC (Dark brown ) 330, Left, RC coil
Widex
FDA UDI
Widex A/S·05706069673333·Widex EVOKE E-CIC (Clay brown ) 330, Left, RC coil
Widex
FDA UDI
Widex A/S·05706069673326·Widex EVOKE E-CIC (Light beige ) 330, Left, RC ...
HOURGLASS
FDA Adverse Event
Injury
·MEDTRONIC·Product code MQP·June 16, 2014
QUATTRODE
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LWS·April 10, 2013
CIDEX PLUS 28 DAY SOLUTION
FDA Adverse Event
Injury
·ADVANCED STERILIZATION PRODUCTS·Product code LRJ·June 12, 2008
CARPENTIER-EDWARDS PERIMOUNT AORTIC PERICARDIAL BIOPROSTHESIS
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code DYE·April 15, 2011
LOGIC CC TIB INSERT SIZE 3, 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 13, 2024
TRULIANT TIB IMP PS INSERT SZ 3 13MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 11, 2024
LOGIC KNEE SYSTEM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·August 18, 2022
LOGIC CC TIB INSERT SIZE 3, 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·March 12, 2024
LOGIC TIBIA IMPLANT PSC INSERT, SZ 3, 15MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·January 20, 2026