216 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ZOLL M SERIES
FDA 510(k)
FDA Class 3
·Cardiovascular
22MM FLEXTUBE BREATHING SYSTEM WITH INTEGRAL MONITORING LINE 1.6M
FDA UDI
Intersurgical Incorporated·05030267152766·22MM FLEXTUBE BREATHING SYSTEM WITH INTEGRAL MO...
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120102571·Steel - Excavating burs
GC RELINE™ II
FDA UDI
Gc America Inc.·D0470102571·GC RELINE™ II Cartridge ExtraExtraSoft: 1 x 55g...
GC RELINE™ II
FDA UDI
Gc America Inc.·14548161321358·GC RELINE™ II Cartridge ExtraExtraSoft: 1 x 55g...
HERMANN MEDIZINTECHNIK GMBH
FDA registration
HERMANN MEDIZINTECHNIK GMBH·69 products·🇩🇪 Germany
FOSTER GRANT
FDA UDI
FGX INTERNATIONAL INC.·00193033119723·
InTess Lumbar Cage
FDA UDI
Kalitec Direct LLC·B07312K0102070·Shaver, Open 7mm
neoWave LS
FDA UDI
XENIX MEDICAL LLC·00818345023901·PADDLE SPREADER, 7MM
IMMULITE 2000 PAP, MODELS L2KPA2, L2KPA6
FDA 510(k)
FDA Class 2
·Clinical Chemistry
INTRACOIL STENT
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
CORE
FDA UDI
STRYKER CORPORATION·04546540667472·U Series Steering Dura Guard
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD/HUNTINGTON·Product code HQL·March 12, 2013
PETITE PACING LEAD
FDA Adverse Event
Malfunction
·OSCOR INC.·Product code DTB·February 11, 2011
VECTRA GENISYS 4 CHANNEL COMBO
FDA Adverse Event
Other
·CHATTANOOGA GROUP·Product code IPF·March 11, 2008
NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 16, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 3, 2026
PANEL PHOENIX NMIC-312
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 23, 2026
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026
BD PHOENIX¿ NMIC-311
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 19, 2026