24 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRECISION VPS IMPRESSION MATERIAL
FDA 510(k)
FDA Class 2
·Dental
NOA Medical Industries, LLC
FDA UDI
Hoffmann NOA Medical Industries, LLC·00817492013162·TRAPEZE - NOA Freestanding
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00400531·
NA
FDA UDI
Stryker GmbH·00886385009131·End Cap, Right A3 Nail 15mm
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450148075·
ACL 9000 SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
HUMI-FLOW, MODEL 6-850-00/ 01/02
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BARREL REAMER ASSEMBLY STANDARD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code LXH·May 17, 2017
BARREL REAMER ASSEMBLY STANDARD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code LXH·May 17, 2017
BARREL REAMER ASSEMBLY STANDARD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code LXH·May 17, 2017
BARREL REAMER ASSEMBLY STANDARD
FDA Adverse Event
Malfunction
·STRYKER GMBH·Product code LXH·May 17, 2017
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 8, 2012
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·September 14, 2012
S5 DOUBLE HEAD PUMP
FDA Adverse Event
Other
·SORIN GROUP DEUTSCHLAND·Product code DTQ·August 29, 2012
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012
S5 CONTROL PANEL
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 15, 2012
S5 CONTROL DISPLAY MODULE
FDA Adverse Event
Malfunction
·SORIN GROUP DEUTSCHLAND·Product code DTQ·May 16, 2012
ALIGN TO URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code FTL·April 3, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC·Product code GJS·March 9, 2011