190 results
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35ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ASTRA & AVANT Navigation Instruments System and ASTRA-OCT Navigation Instruments System
FDA 510(k)
FDA Class 2
·Neurology
n.a.
FDA UDI
Karl Storz GmbH & Co. KG·04048551077146·Sickle Knife, slightly curved, 16 cm
Tripod Wrist Lacer
FDA UDI
MEDICAL SPECIALTIES INCORPORATED·00802357233014·
BIOPHEN ABNORMAL CONTROL PLASMA
FDA UDI
HYPHEN BIOMED·03663537008313·
10PW - Centerpoint Energy
FDA UDI
Certified Safety Manufacturing, Inc.·00766588233017·10PW - Centerpoint Energy
Bordetella immunology reagents IgA
FDA UDI
SAVYON DIAGNOSTICS LTD·07290013348487·Bordetella immunology reagents IgA- IgA Sera pack
Orthopedic Instruments
FDA UDI
GM DOS REIS INDUSTRIA E COMERCIO LTDA·07899258637082·
Portex
FDA UDI
ICU MEDICAL, INC.·15019517086270·
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134873·LATERAL,MUSCLE RETRACTOR,200
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134866·LATERAL,MUSCLE RETRACTOR,180
MST/Dewey 1.1mm A1 Bent Ph Tip 30deg
FDA UDI
MICROSURGICAL TECHNOLOGY, INC.·00844685000364·
InCore Subtalar System
FDA 510(k)
FDA Class 2
·Orthopedic
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM
FDA 510(k)
FDA Class 2
·Microbiology
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 4, 2014
CYPHER SIROLIMUS-ELUTING CORONARY STENT
FDA Adverse Event
Injury
·CORDIS LLC (PR)·Product code NIQ·August 25, 2011
2520274-2013-04176
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·July 12, 2013
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026