32 results · 23ms · Sources: EU EUDAMED, US FDA

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ARSTASIS ONE LATCHWIRE ACCESS SYSTEM

FDA 510(k)
FDA Class 2 ·Cardiovascular

NexxZr™ / W-98-35-UT-C400-ML

FDA UDI
SAGEMAX BIOCERAMICS, INC·00842271139610·

FlexStep

FDA UDI
Liftup A/S·05714420031432·FlexStep V2, 800, 5 step, indoor

PMT CORPORATION - STEREOTACTIC

FDA UDI
PMT CORPORATION·00650551098294·sEEG DEPTH ANCHOR BOLT DRIVER, FOR 2.4MM DRILL BIT

BENZODIAZEPINES

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

MILLENNIUM BLADES, MODEL MB101

FDA 510(k)
FDA Class 1 ·Ophthalmic

PLATE, FIXATION, BONE

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HRS·October 24, 2015

VSP SYSTEM

FDA Adverse Event
Injury ·3D SYSTEMS·Product code DZJ·December 18, 2020

NC TREK CORONARY DILATATION CATHETER

FDA Adverse Event
Injury ·ABBOTT VASCULAR·Product code LOX·December 16, 2022

VA LOCKSCR Ø2.4 SELF-TAP L12 TAN

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·June 18, 2013

SECURE II MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·May 9, 2013

PRECISION®

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 25, 2011

PERFIX PLUG

FDA Adverse Event
Injury ·DAVOL INC., SUB. C.R. BARD, INC.·Product code FTL·August 8, 2008

VA LOCKSCR Ø2.7 HEAD 2.4 SELF-TAP L14 TA

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·April 27, 2022

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HWC·July 30, 2015

SCREW,FIXATION,BONE

FDA Adverse Event
Malfunction ·SYNTHES (USA)·Product code HWC·December 30, 2014

UNK - SCREWS: 2.7 MM VA LOCKING

FDA Adverse Event
Malfunction ·SYNTHES GMBH·Product code HWC·March 1, 2024

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·July 22, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·August 12, 2016

SCREW, FIXATION, BONE

FDA Adverse Event
Injury ·SYNTHES USA·Product code HWC·October 24, 2015