43 results · 23ms · Sources: EU EUDAMED, 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