8 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
ERBE APC RASPATORY HANDLE AND TIP, MODEL 20132-102, 20132-103
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
NeuroOne Cortical Electrode
FDA 510(k)
FDA Class 2
·Neurology
EMERSON 33-AN NEGATIVE PRESSURE RESPIRATOR ALARM
FDA 510(k)
FDA Class 2
·Anesthesiology
BD SAFETYGLIDE¿ INSULIN SYRINGE WITH ATTACHED NEEDLE
FDA Adverse Event
Malfunction
·BD MEDICAL - DIABETES CARE·Product code MEG·April 16, 2018
HERCULES 3 STAGE WIREGUIDED BALLOON ESOPHAGEAL-PYLORIC-COLONIC
FDA Adverse Event
Malfunction
·WILSON-COOK MEDICAL, INC.·Product code KNQ·February 27, 2013
9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·February 4, 2011
PULSE-GENERATOR, DUAL CHAMBER, IMPLANTABLE
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA, INC.·Product code LWP·August 8, 2014
Daig Livewire Steerable, Product Number 401904; REPROCESSED ELECTROPHYSIOLOGY CATHETER
FDA Enforcement
Class II
·Ongoing·Stryker Sustainability Solutions·May 20, 2026