10 results
·
19ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
U&U Insulin Syringe with/without Safety Retractable Device
FDA 510(k)
FDA Class 2
·General Hospital
PILLING
FDA UDI
TELEFLEX INCORPORATED·24026704509045·
LACTOSORB SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036055851·
OMEGA LABORATORIES HAIR DRUG SCREENING ASSAY FOR COCAINE AND COCAINE METABOLITES
FDA 510(k)
FDA Class 2
·Clinical Toxicology
MI VARNISH
FDA 510(k)
FDA Class 2
·Dental
COLLEAGUE PRE-P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 7, 2011
ATTAIN ABILITY
FDA Adverse Event
Injury
·RICE CREEK MFG·Product code OJX·June 8, 2013
SYSTEM, PERITONEAL, AUTOMATIC DELIVERY
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 8, 2014
Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·May 16, 2018
ELEKTA LIMITED Precise Digital Accelerator, REF MRT 6001, MRT 6011; Medical Charged-Particle Radiation Therapy System Accelerator, Linear
FDA Enforcement
Class II
·Ongoing·Elekta, Inc.·December 13, 2023