21 results
·
24ms
·
Sources: EU EUDAMED, US FDA
DSL SEX HORMONE BINDING GLOBULIN (SHBG) (DSL 6300)
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Connector
FDA UDI
ADLER ORTHO SPA·08050507133642·QUICK-COUPLING CONNECTOR FOR HEADLESS NAILS
VuePoint
FDA UDI
Nuvasive, Inc.·00887517178237·VuePoint Plate, 35mm Keel
SureStep™ Foley Tray System
FDA UDI
C. R. Bard, Inc.·00801741104725·SureStep® Foley Tray System (Add-A-Foley Cathet...
Bard® Add-A-Foley Urine Meter Foley Tray
FDA UDI
C. R. Bard, Inc.·00801741040559·Bard® Add-A-Foley Urine Meter Foley Tray
Graft Preparation Table
FDA UDI
Biomet Orthopedics, LLC·00887868511066·
GRAFT PREP TABLE
FDA UDI
Biomet Orthopedics, LLC·00880304405288·
Vitacrilic®
FDA UDI
FRICKE INTERNATIONAL, INC.·B7159041000·Colorstable Extra Fast Self Curing Monomer
INNOFLUOR (TM) AMIKACIN REAGENT SET
FDA 510(k)
FDA Class 2
·Clinical Toxicology
VECTRA(TM)
FDA 510(k)
FDA Class 1
·Ophthalmic
GC Aligner Connect
FDA UDI
Gc Orthodontics America Inc.·E53590410000001·GC Aligner Connect
URINE CONTROL 1, CAT. NO. 903600, URINE CONTROL 2, CAT. NO. 904100
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Truliant
FDA UDI
Exactech, Inc.·10885862585882·TRULIANT PIN PULLER SYRINGE STYLE
EON IMPLANTABLE PULSE GENERATOR
FDA Adverse Event
Injury
·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·October 28, 2010
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 1, 2014
GOBED II MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·November 30, 2012
TRUL FEM IMPACTOR HEAD LOCKING
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code JWH·August 6, 2021
TRULIANT PIN PULLER SYRINGE STYLE
FDA Adverse Event
Malfunction
·EXACTECH, INC.·Product code JWH·August 6, 2021
SureStep(TM) FOLEY TRAY SYSTEM, Preconnected Closed System Foley Tray, Product Codes: A119214M, A119216M, A119218M, A119416M, A153200, A300916A, A301216, A301216A, A303314A, A303316A, A303318A, A303414A, A303416A, A303418A, A304400A, A304714A, A304716A, A304718A, A304914, A304916, A304918, A307414A, A307416A, A319414AM, A319416A, A319416AM, A319418AM, A319514AM, A319516A, A319516AM, A333100A, A333416A, A339414AM, A339516AM, A339516AM, A344916, A800064, A800065, A800364, A800365, A800366, A900216, A900416, A901216, A902114, A902216, A902414, A902416, A902418, A902616, A902914, A902916, A902918, A903314A, A903316A, A903318A, A903416A, A904100, A904400A, A909116M, A909216M, A919416AM, A919516AM, A942206, A942208, A942210, A942212, A942214, A942216, A942218, A942616, A942618, A943214, A943216, A943218, MTA902416 Product Usage catheter
FDA Recall
Terminated
·Bard Medical Division·Product code MJC·December 13, 2018
EXACTECH
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code LXH·October 28, 2021