10,000 results
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43ms
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Sources: EU EUDAMED, US FDA
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868344329·
BIOMET KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304002432·
Biomet® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868344343·
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304435025·
AGC Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304243057·
Eurolink Europe Compliance Limited
Authorized representative
🇮🇪 Ireland·35 Manufacturers·252 Devices
CDS Hematology Calibrator
FDA UDI
CLINICAL DIAGNOSTIC SOLUTIONS, INC.·00812137010421·CDS Hematology Calibrator is manufactured for c...
CDS Hematology Calibrator
FDA UDI
CLINICAL DIAGNOSTIC SOLUTIONS, INC.·00812137010360·CDS Hematology Calibrator is manufactured for c...
MAXIM® KNEE SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00887868225215·
Maxim® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868225208·
Maxim® Knee System
FDA UDI
Biomet Orthopedics, LLC·00887868225222·
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV-ICD System
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV ICD DVEA3E4
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Epsila EV Extravascular Lead
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV ICD, Epsila EV Extravascular Lead
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Epsila EV Extravascular Lead EV2401
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV ICD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV ICD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV-ICD
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·EV ICD - Aurora