11 results
·
26ms
·
Sources: EU EUDAMED, US FDA
AXSYM PROGESTERONE
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Armada
FDA UDI
Nuvasive, Inc.·00887517391865·ARM15S Screw, 5x25mm Fixed
ReLine
FDA UDI
Nuvasive, Inc.·00195377075147·RELINE C Screw, 5.0x25mm Cort Canc
BASE
FDA UDI
Nuvasive, Inc.·00887517701718·BASE HL Trial, 10x38x28mm 25°
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665588029·MIS Fenestrated Screw M, Ø5.0 x 25mm, Ø5.5mm Rod
DIGITAL THERMOMETER KITS
FDA 510(k)
FDA Class 2
·General Hospital
PRISM BONE CEMENT MIXING SYSTEM
FDA 510(k)
FDA Class 1
·Orthopedic
INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·February 11, 2013
RIATA ACTIVE FIXATION
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·January 10, 2011
DIALYZER, HIGH PERMEABILITY WITH OR WITHOUT SEALED DIALYSATE SYSTEM
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CALI·Product code KDI·July 24, 2014
CS Uni-Directional w Auto ID, Product Number D135304; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026