17 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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RADIFORCE GX220 AND GS220 MONOCHROME LCD MONITORS
FDA 510(k)
FDA Class 2
·Radiology
Dalbo®-Z / Dalbo®-B / Profix / Pro-Snap
FDA UDI
Cendres+Métaux SA·07640166514312·Dalbo®-Z / Dalbo®-B / Profix / Pro-Snap
Paralle...
Paltop
FDA UDI
PALTOP ADVANCED DENTAL SOLUTIONS LTD·07290108696295·Nylon Ball Abutment Retentive Cap Very Elastic ...
Thermaloy
FDA UDI
Rmo, Inc.·00885797021168·THERMALOY PLUS PREFORMED EXPANDED ARCH MX/MN .0...
Varnish America
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·00302730002447·VarnishAmerica 5% Sodium Fluoride Varnish, 0.25...
Varnish America 0.25ml Box / 200 White Raspberry
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·10302730701316·0.25ml Box / 200 count
DENTAL ATTACHMENTS
FDA UDI
RHEIN 83 SRL·08059224192079·DISPOSABLE device in plastic material to be emb...
Cordant
FDA UDI
Seaspine Orthopedics Corporation·10889981115197·31mm
BD BBL¿ TRYPTICASE¿ SOY BROTH
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·June 30, 2021
BD BBL¿ TRYPTICASE¿ SOY BROTH
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·June 25, 2021
PHD PERSONAL HEMODIALYSIS INSTRUMENT-1M101, PHD WATER PRE-TREATMENT KIT-1W605,PHD HARD PLUMBING KIT-1W604, PHD BLOOD TUB
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
QUICKSCREEN PRO MULTI DRUG SCREENING TEST, MODEL 9153 PAT04
FDA 510(k)
FDA Class 2
·Clinical Toxicology
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·June 4, 2007
ARCHITECT CA 125 II
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code LTK·April 22, 2013
INFINITI VISION SYSTEM OZIL
FDA Adverse Event
Injury
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·April 22, 2011
INFINITI VISION SYSTEM
FDA Adverse Event
Malfunction
·ALCON - IRIVINE TECHNOLOGY CENTER·Product code HQC·July 3, 2008
BD BBL¿ TRYPTICASE¿ SOY BROTH
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code JSG·June 29, 2021