25 results
·
23ms
·
Sources: EU EUDAMED, US FDA
CosmoLock Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07311K0310080·Probe, 1.5 inch Ball, Lenke, Thoracic, Straight...
AESCULAP NEURO PATTIES, NEUROSORB 4, 6, AND 75 (GREEN & WHITE)
FDA 510(k)
FDA Class 2
·Neurology
AOS CORTICAL SCREW, LOW PROFILE 3.5mm x 8mm
FDA UDI
ADVANCED ORTHOPAEDIC SOLUTIONS, INC.·00848665009248·
EVOS Lumbar Interbody System
FDA UDI
Cutting Edge Spine, LLC·00841193107707·HA PEEK EVOS Straight, ,8mmx11mmx 30mm , FLAT 5...
IVF HARTMANN AG
FDA registration
IVF HARTMANN AG·1 product·🇨🇭 Switzerland
K032008
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC·Product code LJT·May 31, 2007
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710620310080·Quad Channel Met-Traverse, 31mm x 8mm
Intelliguides
FDA UDI
Mios Marketing, LLC·G2710610310080·Tri-Channel Met-Traverse, 31mm x 8mm
NEXUS 2 MODIFIED
FDA 510(k)
FDA Class 2
·Dental
TEMPTELLER INFRARED EAR THERMOMETER, MODELS TT-901, TT-911 AND TT-921
FDA 510(k)
FDA Class 2
·General Hospital
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·April 2, 2019
SEE H10
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·March 28, 2013
ACCU-CHEK SPIRIT
FDA Adverse Event
Injury
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·March 16, 2011
GE OEC 9900
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·April 17, 2008
ALINITY M RESP-4-PLEX AMP KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025
ALINITY M RESP-4-PLEX AMP KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025
ALINITY M RESP-4-PLEX AMP KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025
ALINITY M RESP-4-PLEX AMP KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025
ALINITY M RESP-4-PLEX AMP KIT
FDA Adverse Event
Malfunction
·ABBOTT MOLECULAR, INC.·Product code QJR·September 16, 2025