28 results
·
28ms
·
Sources: EU EUDAMED, US FDA
CATHETER REPAIR KIT WITH REPLACEMENT CONNECTOR, MODEL 5587000
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ROLLO 110X25X16E/QT-HS/RED GRID
FDA UDI
AB MEDICA GROUP, S.A.·08428763052401·
MYELO-NATE
FDA UDI
UTAH MEDICAL PRODUCTS, INC.·H67140110150·MYELONATE KIT (1") 22GA
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193106410·HA PEEK EVOS Straight, ,15mmx11mmx 30mm , FLAT ...
ORTHOPEDIC MANUAL SURGICAL INSTRUMENT
FDA UDI
FX SOLUTIONS·03701037313695·STABILITY TRIAL CUP Ø32 + 15
RINGFIX
FDA UDI
Stryker GmbH·00886385009919·Half-Pin Surgical Tray
Single Use Biliary Stent V
FDA UDI
OLYMPUS MEDICAL SYSTEMS CORP.·04953170186011·Single Use Biliary Stent V
ELECSYS THYROGLOBULIN CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
INSTANT-VIEW METHADONE URINE CASSETTE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·July 2, 2025
AUTOSOFT 90
FDA Adverse Event
Malfunction
·UNOMEDICAL DEVICES S.A. DE C.V.·Product code FPA·June 17, 2025
SCREW LOCKING
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES OBERDORF·Product code HWC·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HRS·March 14, 2012
SCREW
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HWC·March 14, 2012
PADGETT MODEL S LIMLINE ELECTRIC DERMATOME
FDA Adverse Event
Injury
·INTEGRA LIFESCIENCES CORPORATION (INTEGRA-OHIO)·Product code GFD·March 11, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·March 8, 2011
IDENTITY DR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DXY·March 10, 2008
3.5MM TI LCP® PROXIMAL HUMERU PLATE-STANDARD 3H SHAFT/90MM
FDA Adverse Event
Injury
·SYNTHES RARON·Product code KTW·February 16, 2016