10,000 results
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125ms
·
Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FDA UDI
SOUTHERN IMPLANTS (PTY) LTD·06009544027867·Quad Gold Screw for Int. Hex
Antiserum, Vibrio Cholerae, All Varieties
FDA classification
FDA Class 2
·Antiserum, Vibrio Cholerae, All Varieties
GSI CORP.
FDA registration
GSI CORP.·2 products·🇺🇸 United States
GSB LLC
FDA registration
GSB LLC·1 product·🇺🇸 United States
NATIONAL DISTRIBUTION & CONTRACTING INC.
FDA UDI
NORDENT MANUFACTURING INC·00840018601680·CONDNSER #0/1 SERR QUALA
SHENZHEN GSD TECH CO., LTD
FDA registration
SHENZHEN GSD TECH CO., LTD·5 products·🇨🇳 China
GSO GS1 SPACER
FDA 510(k)
FDA Class 2
·Orthopedic
NATIONAL DISTRIBUTION & CONTRACTING INC.
FDA UDI
NORDENT MANUFACTURING INC·00840018601888·BARNHART CURET #1-2 QUALA S HND
NATIONAL DISTRIBUTION & CONTRACTING INC.
FDA UDI
NORDENT MANUFACTURING INC·00840018602045·GRACEY 1/2 CURET QUALA S HND
GSO GS1 SPINAL SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Midmark
FDA UDI
MIDMARK CORPORATION·00841709113109·
GSO GS1 CANNULATED SCREW SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
VENOUS HARDSHELL CARDIOTOMY RESERVOIR W/SAFELINE COATING, MODEL BSQ-VHK 2000;VACUUM TIGHT, MODEL BSQ-VHK 2001
FDA 510(k)
FDA Class 2
·Cardiovascular
Fountain®
FDA UDI
Merit Medical Systems, Inc.·00884450012277·
Fountain®
FDA UDI
Merit Medical Systems, Inc.·00884450825983·
Fountain®
FDA UDI
Merit Medical Systems, Inc.·00884450011638·
THERMACOOL
FDA Adverse Event
Malfunction
·THERMAGE·Product code GEI·December 22, 2005
BD PROBETEC NEISSERIA GONORRHOEAE (GC) Q AMPLIFIED DNA ASSAY
FDA 510(k)
FDA Class 2
·Microbiology
AMBULIFT BSQ
FDA Adverse Event
Other
·ARJO LTD.·Product code FSA·July 26, 2000
AMBULIFT BSQ
FDA Adverse Event
Malfunction
·ARJO LTD.·Product code FSA·October 30, 2001