38 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MONARCH NASAL IMPLANT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
BioQuick®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70710181·BioQuick-Brackets Roth .018" 5 cases Starter-as...
Imola-Silverstone
FDA UDI
Altus Spine, LLC·00843210134000·SS Paddle Distractor 18mm
General Instrument
FDA UDI
ORTHOPEDIATRICS CORP.·00841132127179·Double Drill Guide 4.5mm and 2.8mm
NA
FDA UDI
STRYKER CORPORATION·04546540077288·1.8mm x 11.0mm Tapered Router
TAUT BALLOON CATHETER, MODEL 50640
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MICROSCAN MICROSTREP PLUS PANEL - CHLORAMPHENICOL
FDA 510(k)
FDA Class 2
·Microbiology
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 26, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 ROLLER PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 6, 2012
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
S5 SYSTEM
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·July 27, 2010
COCR FEMORAL HEAD
FDA Adverse Event
Injury
·ZIMMER MANUFACTURING B.V.·Product code LPH·February 23, 2018
S5 SENSOR MODULE FOR BUBBLE DETECTOR
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTW·October 21, 2016
VERSACARE BED
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·April 8, 2013
MESH - COMPOSIX
FDA Adverse Event
Injury
·DAVOL INC.·Product code FTL·April 19, 2011