17 results
·
24ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BARD 3DMAX MESH
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Stamey
FDA UDI
COOK INCORPORATED·00827002140981·Stamey Percutaneous Suprapubic Catheter Set
miniARM® multiSTATION™ System
FDA UDI
LSI Solutions, Inc.·00850012846093·M45™ CLICK RELEASE™ miniARM® Holder
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193110417·HA PEEK EVOS Rotate, , 10mmx8mmx 30mm , FLAT 8 ...
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014608907·MIDMARK 3.25" DELUXE GEL
APEX Knee System
FDA UDI
Omni Life Science, Inc.·00841690110248·Tibial Cutting Block Utube
N.A.
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR76000810101·Lingual cleat
ASCENT KNEE REVISION FEMORAL STEM
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFIED CARDIAC CRYOSURGICAL SYSTEM, MODELS 6TCS1 & 6TCSE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 5, 2024
REMSTAR AUTO M SERIES
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·April 14, 2024
840 VENTILATOR
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY NELLCOR PURITAN·Product code CBK·April 24, 2013
HEARTSINE SAMARITAN 300P AND PAD PAK
FDA Adverse Event
Malfunction
·HEARTSINE TECHNOLOGIES, LTD, CANBERRA HOUSE·Product code MKJ·August 11, 2014
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 14, 2011
HOSP SS FLEXX METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·February 22, 2011
HOSP SS FLEXX METER W/O LASER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·May 17, 2011
HOSP SS FLEXX METER
FDA Adverse Event
Death
·LIFESCAN INC.·Product code NBW·April 1, 2011