10 results
·
18ms
·
Sources: EU EUDAMED, US FDA
MODEL 2000W OPTION H CONFIGURATION
FDA 510(k)
FDA Class 2
·Anesthesiology
KMEDIC
FDA UDI
TELEFLEX INCORPORATED·24026704293289·
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690117919·MODULAR TIBIA PUNCH DART Size 5-6
K-Wire w. double end trocarpoint 1.1mm/229mm, 6 pcs./unit
FDA UDI
mahe medical gmbh·EMAHKM713020·K-Wire w. double end trocarpoint
1.1mm/...
PFISTER-SCHWARTZ STONE RETRIEVER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NEUROSTAT, LLOYD
FDA 510(k)
FDA Class 2
·Neurology
HS III PROXIMAL SEAL SYSTEM 3.8MM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code DXC·April 15, 2014
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 13, 2012
PINN MAR +4 10D 28IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 15, 2010
Azurion 7 M20; Catalog numbers: (1) 722079, (2) 722224, (3) 722234, (4) 722282 (OUS ONLY);
FDA Enforcement
Class I
·Ongoing·PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.·February 26, 2025