31 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ACTABOND Topical Skin Adhesive
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HUDSON 22MM DUAL HTD CIRC KIT
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·February 19, 2016
HUDSON 22MM DUAL HTD CIRC KIT
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·February 19, 2016
HUDSON 22MM DUAL HTD CIRC KIT
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·February 19, 2016
HUDSON 22MM DUAL HTD CIRC KIT
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BTT·February 19, 2016
CoRoent
FDA UDI
Nuvasive, Inc.·00887517291998·CoRoent® XLFW, 10x22x50mm
LoFric® Sense™
FDA UDI
Wellspect AB·07333387021881·Single Use Urinary Catheter LoFric Sense Nelato...
LoFric® Sense™
FDA UDI
Wellspect AB·07392532086168·Single Use Urinary Catheter LoFric Sense Nelato...
CoRoent
FDA UDI
Nuvasive, Inc.·00887517731029·CoRoent XL+, 10x18x50mm 15°
MEGA SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809763501296·Mono Screw Driver
A.D. Protraction
FDA UDI
ORMCO CORPORATION·00889989060003·International Face Mask Blue
Vilex Power Accessory
FDA UDI
VILEX IN TENNESSEE, INC.·00841731122254·KWire .062x4" (1.6x100mm)
Kyocera Medical Technologies, Inc.
FDA UDI
KYOCERA MEDICAL TECHNOLOGIES, INC.·00841523104024·T³ Acetabular Hemispherical Shell, Cluster Hole...
GYNECARE MORCELLEX TISSUE MORCELLATOR, MODELS MX0100 AND MX0100R
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ESOPHAGEAL / RECTAL TEMPERATURE PROBE, 9FR, 12FR, ESOPHAGEAL STETHOSCOPE WITH TEMPERATURE SENSOR, 9FR, 12FR, 18FR, 24FR
FDA 510(k)
FDA Class 2
·Anesthesiology
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·October 10, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013
UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code MMI·June 17, 2011
COMP RVRS SHLDR GLNSP +6 36MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 12, 2018
ARCOM XL 44-36 RTNV+3 HMRL BRG
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KWS·December 12, 2018