10 results
·
35ms
·
Sources: EU EUDAMED, US FDA
CK-UV REAGENT
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Tranquil-L™
FDA UDI
NEXUS SPINE, L.L.C.·B6788232110·DLIF Inserter Spanner Wrench
Legacy™2 Implant
FDA UDI
IMPLANT DIRECT SYBRON MANUFACTURING LLC·10841307101208·Ø3.2 x 11.5 Platform 3.0mmD
NEXGEN COMPLETE KNEE SOLUTION CRUCIATE RETAINING (CR)-FLEX FEMORAL COMPONENTS
FDA 510(k)
FDA Class 2
·Orthopedic
A5 ANESTHESIA DELIVERY SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
I-STAT CG8+ CARTRIDGE
FDA Adverse Event
Malfunction
·ABBOTT POINT OF CARE·Product code CHL·December 22, 2021
BEMIS 1200CC HIFLOW SUCTION CANISTER
FDA Adverse Event
Malfunction
·BEMIS MFG. CO.·Product code GCX·February 27, 2014
ARTHROSCOPE
FDA Adverse Event
Malfunction
·MDT KYPHON NEUCHATEL MFG·Product code HRX·November 7, 2012
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code MDS·September 1, 2010
Various convenience packs
FDA Enforcement
Class II
·Ongoing·American Contract Systems, Inc.·September 14, 2022