33 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAREMATIX WELLNESS SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
LoFric®
FDA UDI
Wellspect AB·07333387038094·Single Use Urinary Catheter LoFric Nelaton 8" 18FR
LoFric®
FDA UDI
Wellspect AB·07392532135279·Single Use Urinary Catheter LoFric Nelaton 8" 18FR
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR20318401·BioStarter wires Euro-Smile-F. max. .016"
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102237·SLOANE LASEK MICRO HOE
Disposable Silicone Foley Catheter
FDA UDI
Guangdong Baihe Medical Technology Co., Ltd.·06938634494893·
LEKON
FDA UDI
C A I INDUSTRIES CORP·00807689003120·
CERVILENZ UTERINE MEASURING SOUND
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
MICROJET CRONO PAR AND CRONO APO-GO
FDA 510(k)
FDA Class 2
·General Hospital
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDIC, INC.·Product code KWP·March 15, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·September 26, 2016
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·July 26, 2016
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 11, 2017
APPLIANCE, FIXATION, SPINAL INTERLAMINAL
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·October 25, 2017
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·April 4, 2016
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Malfunction
·WARSAW ORTHOPEDICS·Product code KWP·April 6, 2017
SENSOR ENLITE
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OZO·August 26, 2015
HOMECHOICE PRO
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·April 3, 2013
GO BED PLUS
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·February 25, 2011
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDICS·Product code KWP·February 7, 2020