99 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC AVE BRIDGE EXTRA SUPPORT OVER THE WIRE RENAL STENT SYSTEM
Stent, Renal
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC AVE BRIDGE EXTRA SUPPORT OVER-THE-WIRE RENAL STENT SYSTEM
Promolux Polymer pink
FDA UDI
Merz Dental GmbH·D7091020007·Promolux Polymer pink, 100g
EverFlo
FDA UDI
Respironics, Inc.·00606959032569·EverFlo w/Oxygen Percentage Indicator, 230V, IKK
HEMO-NATE
FDA UDI
UTAH MEDICAL PRODUCTS, INC.·H67140200070·FILTER SET, Syringe Infusion Set with a Microag...
FJ2000 System
FDA UDI
Paragon 28, Inc.·00889795131263·FJ-2000, Foot Hook
VADER Pedicle System, Rod, Carbon/PEEK, Straight, Ø 6.0 r000 x 070 mm
FDA UDI
icotec AG·07640172551646·VADER Pedicle System, Rod, Carbon/PEEK, Straigh...
A8 INTEGR8® Porous Pedicle Screw System
FDA UDI
ALLUMIN8, INC.·00850080774137·MINI Reducer Wrench
ROSA® Persona TKA cut guide - A
FDA UDI
Orthosoft Inc·00889024505179·
SAFYRE SLING SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Replacement Heart-Valve
FDA Pre-Market Approval
FDA Class 3
·EDWARDS PRIMA PLUS STENTLESS BIOPROSTHESIS MODEL 2500P
Kit, Test, Alpha-Fetoprotein For Neural Tube Defects
FDA Pre-Market Approval
FDA Class 3
·IMMULITE/IMMULITE 1000 AFP AND IMMULITE 2000/IMMULITE 2500 AFP
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·June 8, 2013
UNKNOWN CAS PIN
FDA Adverse Event
Malfunction
·ZIMMER CAS·Product code OLO·May 29, 2025
ACTIVA
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MRU·July 8, 2019
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code MRU·July 25, 2019
UNKNOWN PIN
FDA Adverse Event
Malfunction
·ZIMMER CAS·Product code OLO·June 16, 2025
XIENCE PRIME EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·AV-TEMECULA-CT·Product code NIQ·March 25, 2013
MICROVASIVE GOLD PROBE
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC - MIAMI·Product code KNS·March 16, 2011
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 19, 2014