32 results
·
61ms
·
Sources: EU EUDAMED, US FDA
Alinity c ICT Sample Diluent (LN 07P5320)
FDA registration
ABBOTT LABORATORIES·3 products·🇺🇸 United States
Alinity c ICT Sample Diluent (LN 07P5320)
FDA registration
ABBOTT LABORATORIES·3 products·🇺🇸 United States
Alinity c ICT Sample Diluent
FDA registration
Fisher Diagnostics·3 products·🇺🇸 United States
Alinity c ICT Sample Diluent
FDA 510(k)
FDA Class 2
·Clinical Chemistry
Electrode, Ion-Specific, Chloride
FDA classification
FDA Class 2
·Electrode, Ion-Specific, Chloride
ACS
FDA UDI
AMERICAN CONTRACT SYSTEMS, INC.·00191072017420·PLASTIC SURGERY PACK - 170320
Responsive Orthopedics Total Knee Arthroplasty System
FDA UDI
RESPONSIVE ORTHOPEDICS, LLC·00841973107361·TRIAL 90-SRK-170320 POLY UCCS 3X20MM
INTEGRAL X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182547·
LAMP-C
FDA registration
Covidien·2 products·🇮🇪 Ireland
LAMP-C
FDA registration
Covidien·2 products·🇺🇸 United States
US/JAP 110V PSU
FDA registration
CHINA TURNKEY SOLUTIONS LOGISTICS (SHENZHEN) CO., LTD.·1 product·🇨🇳 China
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003289·MCK PATELLA DOME TRIAL (38mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003265·MCK PATELLA DOME TRIAL (32mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003258·MCK PATELLA DOME TRIAL (29mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003296·MCK PATELLA DOME TRIAL (41mm)
INTEGRAL X-SERIES HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304182257·
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003241·MCK PATELLA DOME TRIAL (26mm)
RESTORIS
FDA UDI
MAKO SURGICAL CORP.·00848486003272·MCK PATELLA DOME TRIAL (35mm)
Initial Placement Gastrostomy Set
FDA registration
Cook Incorporated·1 product·🇺🇸 United States
Initial Placement Gastrostomy Set
FDA registration
COOK INCORPORATED·1 product·🇺🇸 United States