39 results · 29ms · Sources: EU EUDAMED, US FDA

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INDOXYL ACETATE DISK

FDA 510(k)
FDA Class 1 ·Microbiology

Ophthalmic Knife

FDA UDI
KATENA PRODUCTS, INC.·00841668101179·GILL CORNEAL KNIFE STRAIGHT

Instrument Case

FDA UDI
KATENA PRODUCTS, INC.·00841668111031·INSTRUMENT CADDY LARGE

FORE-SIGHT ELITE ABSOLUTE TISSUE OXIMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

PVS 1600 SYNCHRO 0.010 NEURO GUIDE WIRE

FDA 510(k)
FDA Class 2 ·Cardiovascular

NONE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code DQX·September 3, 2008

SYNCHRO 14 NEURO GUIDEWIRE

FDA Adverse Event
Injury ·NEUROVASCULAR, A DIVISION OF BOSTON SCIENTIFIC CORPORATION·Product code DQX·July 24, 2007

SYNCHRO -10 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIV·Product code DQX·December 15, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·NEUROVASCULAR , A DIV. OF BOSTON SCIENTIFIC CORP·Product code DQX·December 19, 2006

SYNCHRO 14 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROCASCULAR DIVISION·Product code DQX·August 16, 2007

SYNCHRO .014 GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP. / NEUROVASCULAR DIV.·Product code DQX·August 16, 2007

BD FACSCALIBUR¿ FLOW CYTOMETER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON AND COMPANY, BD BIOSCIENCES·Product code GKZ·January 31, 2023

SYNCHRO -14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP., NEUROVASCULAR DIVISION·Product code DQX·November 30, 2006

SYNCHRO-14 NEURO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION, NEUROVASCULAR DIVISION·Product code DQX·September 12, 2007

SYNCHRO GUIDEWIRE

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORP.·Product code DQX·October 16, 2009

6F ANGIO-SEAL VASCULAR CLOSURE DEVICE VIP

FDA Adverse Event
Injury ·ST. JUDE MEDICAL PUERTO RICO, B.V.·Product code MGB·December 9, 2010

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·January 22, 2013

530G INSULIN PUMP

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZO·July 9, 2014

SYNCHRO 14 "S" NEURO GUIDEWIRE

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC CORP.·Product code DQX·September 20, 2007