588 results
·
22ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 2
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ZYMUTEST HIA IGGAM, ZYMUTEST IGG, MODEL RK040D, RK040A
FDA 510(k)
FDA Class 2
·Hematology
URIC ACID STANDARD SOLUTION CALIBRATOR
FDA 510(k)
FDA Class 2
·Clinical Chemistry
OVAL SHAPES
FDA 510(k)
FDA Class 2
·Orthopedic
SINGLE SIZE TENDON SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
H-H HUNTER ACTIVE TENDON IMPLANT DC
FDA 510(k)
FDA Class 2
·Orthopedic
AVANTA ORTHOPAEDICS TENDON SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
PHOENIX BONE SCREWS PBS-TYPE SERIES
FDA 510(k)
FDA Class 2
·Orthopedic
TENDON ROD MODEL OR41PO3-6
FDA 510(k)
FDA Class 2
·Orthopedic
H-H HUNTER ACTIVE TENDON IMPLANT BC
FDA 510(k)
FDA Class 2
·Orthopedic
PASSIVE TENDON IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
H-H HUNTER ACTIVE TENDON IMPLANT PC
FDA 510(k)
FDA Class 2
·Orthopedic
H-H HUNTER ACTIVE TENDON IMPLANT
FDA 510(k)
FDA Class 2
·Orthopedic
Universal Tendon Spacer
FDA 510(k)
FDA Class 2
·Orthopedic
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·USCI(R) PROBE III(TM) BALLOON-ON-A-WIRE(TM) D. SYS
HemosIL Liquid Anti-Xa
FDA 510(k)
FDA Class 2
·Hematology
INNOVANCE Anti-Xa (OPPU05); INNOVANCE Apixaban Standards (OPPW05); INNOVANCE Apixaban Controls (OPPS05)
FDA 510(k)
FDA Class 2
·Hematology
HemosIL Liquid Anti-Xa
FDA 510(k)
FDA Class 2
·Hematology