15 results
·
20ms
·
Sources: EU EUDAMED, US FDA
OMNI-TRAC MODIFICATION
FDA 510(k)
FDA Class 2
·Cardiovascular
ReLine
FDA UDI
Nuvasive, Inc.·00195377070470·RELINE C Screw, 5.0x20mm MA Thoracic
OMNI Knee
FDA UDI
Omni Life Science, Inc.·00841690101208·Congruent Tibial Insert, Size 2 x 10mm
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955939297·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955938122·Percutaneous Transluminal Angioplasty Balloon C...
JADE PLUS PTA Balloon Dilatation Catheter / JADE PLUS 18 OTW
FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955936951·Percutaneous Transluminal Angioplasty Balloon C...
NA
FDA UDI
Zimmer, Inc.·00889024077898·
NA
FDA UDI
Zimmer, Inc.·00889024103825·
SLIDEX STREPTO-KIT
FDA 510(k)
FDA Class 1
·Microbiology
TRACHEOSTOMY CARE KIT (STERILE)
FDA 510(k)
FDA Class 2
·Anesthesiology
NA
FDA UDI
Zimmer, Inc.·00889024077881·
APEX KNEE SYSTEM
FDA Adverse Event
Injury
·OMNILIFE SCIENCE INC.·Product code JWH·April 11, 2023
ACCESS® 2 IMMUNOASSAY SYSTEM
FDA Adverse Event
Malfunction
·BECKMAN COULTER INC.·Product code LTJ·December 21, 2010
NOVA MAX PLUS GLUCOSE MONITOR
FDA Adverse Event
Malfunction
·NOVA BIOMEDICAL CORP.·Product code NBW·January 25, 2013
PINNACLE SECTOR II CUP 52MM
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code KWA·July 15, 2014