43 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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EMBRYON SINGLE AND DOUBLE LUMEN NEEDLES
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
8000205
FDA UDI
LASER PERIPHERALS, LLC·00816469021407·LaseGuide™ Edge 365u Laser Fiber PL
ACE
FDA UDI
ACE SURGICAL SUPPLY CO., INC.·00614950016556·CURETTE BONE MILLER #11 D/E 7" 18CM TIP SIZE AP...
MTI
FDA UDI
Medical Technology Industries, Inc.·10840118404829·Exam Light, 32" LUMERUS LED Back Mtd, IEC 320 Plug
ISOLA
FDA UDI
DEPUY SPINE, LLC·10705034005706·ISOLA SPINE SYSTEM OPEN HOOK 6.35 x 6.5mm
PRCT2
FDA UDI
FX SOLUTIONS·03701037301852·DIAPHYSEAL PLATE TA6V 5 HOLES
SR Facebow
FDA UDI
ORMCO CORPORATION·00889989023169·Facebow LONG SZ 5 .044 DIA.
SILVERVENT
FDA UDI
Andreas Fahl Medizintechnik-Vertrieb GmbH·04051948000207·SILVERVENT 2 IC, SIZE 5
Matrix Wearable
FDA UDI
GLOBAL INSTRUMENTATION, LLC·00815187020570·M5 Neck Lanyard
FlowLogic Agile
FDA UDI
SONENDO, INC.·00810209420109·FlowLogic Agile Shaping File 15/.06, 21mm
MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (38 CM), MODEL 3555-38; MEDTRONIC EXTENSION PASSER TUNNELING SYSTEM (60 CM),
FDA 510(k)
FDA Class 2
·Neurology
IMMULITE VALPROIC ACID, IMMULITE 2000 VALPROIC ACID, CATALOG # LKVA1, LKVA5 & L2KVA2, L2KVA6
FDA 510(k)
FDA Class 2
·Clinical Toxicology
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·May 17, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·May 17, 2021
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·May 17, 2021
DELTA-TT ACETAB.CUP 52 MM
FDA Adverse Event
Injury
·LIMACORPORATE SPA·Product code LPH·September 25, 2020
LUMIRADX SARS-COV-2 AG TEST STRIP KIT
FDA Adverse Event
Malfunction
·LUMIRADX UK LTD.·Product code QKP·May 17, 2021
XMAX MOTOR
FDA Adverse Event
Malfunction
·THE ANSPACH EFFORT, INC.·Product code ERL·February 14, 2013
RENAISSANCE 29 P-WASH
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FPO·February 3, 2011
8010042-2008-00009
FDA Adverse Event
Malfunction
·Product code CBK·January 23, 2008