26 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IPL hair removal machine
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NA
FDA UDI
Synthes GmbH·10886982153074·3.5MM LOCKING SCREW SELF-TAPPING 20MM
Needle aspiration and injection
FDA UDI
KATENA PRODUCTS, INC.·00841668113615·PERIBULBAR NEEDLE 23GA 32MM
MATIRA ANTERIOR CERVICAL SYSTEM
FDA UDI
Kalitec Direct LLC·B07307K0130201·PLATE CALIPER
Best Medical International
FDA UDI
BEST MEDICAL INTERNATIONAL, INC.·00841365115721·
TruEase
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730012807·TruEase LP Tube 018 LR Bond Sgl NonConv MBT Rx ...
Neptune E-SEP
FDA UDI
STRYKER CORPORATION·07613327297942·Neptune E-SEP Conization Electrode W13 D20 L120
TruFit 2.0
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730033529·TruFit™2.0 .018 MC LR6/7 NC SBT -10T 0O WLD (10PK)
TruEase™
FDA UDI
Ortho Organizers, Inc.·00190707191436·TruEase LP Tube 018 LR Bond Sgl NonConv MBT Rx ...
TruFit™
FDA UDI
Ortho Organizers, Inc.·00190707191887·TruFit 2.0 018 MC LR6/7 NC SBT -10T 0DOff DB (1...
GLOBAL AP
FDA UDI
DEPUY (IRELAND)·10603295090809·GLOBAL AP OSTEOTOME GUIDE PIN 3.2mm LONG
IMMULISA ENHANCED (TM) CARDIOLIPIN IGA, IGG, IGM AND IGA/IGG/IGM ANTIBODY (ACA) ELISAS
FDA 510(k)
FDA Class 2
·Immunology
BLIP MODEL BP-700WF
FDA 510(k)
FDA Class 2
·Cardiovascular
SAFESTEP 22G X 3/4 STRAIGHT
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD)·Product code FPA·March 20, 2009
SAFESTEP 22G X 3/4 STRAIGHT
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD)·Product code FPA·March 20, 2009
BIOGX SARS-COV-2 OPEN SYSTEM REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·February 8, 2021
BD SARS-COV-2 REAGENTS FOR BD MAX SYSTEM
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO. (SPARKS)·Product code QJR·February 16, 2021
ENSITE CLASSIC SYSTEM
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code DQK·February 9, 2010
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITJ·October 30, 2014
INTELLIVUE MULTI MEASUREMENT SEVER X2
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS·Product code MHX·August 9, 2011