42 results
·
27ms
·
Sources: EU EUDAMED, US FDA
THERIFIL BONE FILLER
FDA 510(k)
FDA Class 2
·Orthopedic
Cetro America Ultrasound Transducer 1.5 Mhz for Oxford SonicAid
FDA UDI
CETRO AMERICA INC·00852519007175·Replacement Ultrasound Transducer 1.5 Mhz for O...
ODYSSEY®
FDA UDI
Microport Orthopedics Inc.·M684K00310401·
LoFric®
FDA UDI
Wellspect AB·07333387036922·Single Use Urinary Catheter LoFric Nelaton 8" 10FR
LoFric®
FDA UDI
Wellspect AB·07392532135255·Single Use Urinary Catheter LoFric Nelaton 8" 10FR
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 40mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665009408·
Cosmolock
FDA UDI
Kalitec Direct LLC·B07311K0130400·ROD REDUCER, AXIAL
LIGHT SABER INTRODUCER NEEDLE
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
CRYOCARE CARDIAC SURGICAL SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MATRIX DETACHABLE COILS
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - CORK·Product code HCG·October 12, 2010
8.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
5.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV.·Product code BTR·September 17, 1999
5.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
8.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV.·Product code BTR·September 17, 1999
9.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
6.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
7.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
5.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
9.0MM HI LO
FDA Adverse Event
Malfunction
·MMJ SA DE CV·Product code BTR·September 17, 1999
GDC DETACHABLE COIL
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code HCG·November 23, 2009