9 results
·
27ms
·
Sources: EU EUDAMED, US FDA
ASPIR-PULSE(TM) SAF-T-VENT
FDA 510(k)
FDA Class 1
·Anesthesiology
VARIAX
FDA UDI
Stryker GmbH·07613327370478·F&A Instruments Tray, Insert
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665586940·MIS Cannulated Screw M, Ø10.5 x 75mm, Ø5.5mm Rod
PHARMATECH MENOPAUSE CHECK, MODELS 9111 AND 9112
FDA 510(k)
FDA Class 1
·Clinical Chemistry
ENGSTROM CARESTATION, ENGSTROM PRO
FDA 510(k)
FDA Class 2
·Anesthesiology
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 18, 2014
EON
FDA Adverse Event
Injury
·ST. JUDE MEDICAL- NEUROMODULATION·Product code LGW·January 29, 2013
EXTERNAL NEUROSTIMULATOR
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·December 17, 2010
CS Uni-Directional w Auto ID, Product Number D135303; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026