10 results
·
20ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
KERICURE ADVANCED LIQUID BANDAGE, NATURAL SEAL LIQUID BANDAGE, LIQUID BANDAGE
FDA 510(k)
FDA Class 1
·General Hospital
Sasmar Vanilla
FDA UDI
Sasmar Pharmaceuticals SPRL·09337213008266·PERSONAL LUBRICANT
ArgenIS
FDA UDI
ARGEN CORPORATION, THE·D818131384·MUA AO WP 2.5GH Str Dental implant suprastructu...
LINK Instruments - Drills, reamers and saw blades
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575325672·Orthopaedic prosthesis instrument, reusable - G...
MULTIPLE PRIVATE LABELED, NON-STERILE, POWDER-FREE, POLYURETHANE WHITE COLOR, EXAMINATION GLOVES (INTACTA POLYURETHANE G
FDA 510(k)
FDA Class 1
·General Hospital
LIFEBRIDGE
FDA 510(k)
FDA Class 2
·Cardiovascular
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 3, 2024
COBAS 8000 COBAS ISE MODULE (DOUBLE)
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 1, 2014
APPOSE ULC 35 WIDE SKIN STAPLER
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY NELLCOR·Product code GDT·May 13, 2013
ASKU
FDA Adverse Event
Malfunction
·MEDTRONIC MILACA INC.·Product code DTE·June 16, 2011