8 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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OpClear Platform (CU3 DI3), OpClear Control Unit with Footswitch (CS-CU33), OpClear Disposable Procedure Kits (CS-10-00-300, CS-10-30-300, CS-10-00-315, CS-10-30-315, CS-10-00-330, CS-10-30-330, CS-05-00-290, CS-05-30-290), Contd from 3 above: CS-05-00-300, CS-05-30-300, CS-05-00-315, CS-05-30-315
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
TASMIN R 22°
FDA UDI
SIGNUS Medizintechnik GmbH·04047844015179·The basic shape of the TASMIN R devices is a ho...
Potts Liver Transplant Clamp 26cm Special design acc. to drawing
FDA UDI
Geister Medizintechnik GmbH·04057034059548·Potts Liver Transplant Clamp 26cm
Specia...
DYNALINK .035 BILIARY SELF-EXPANDING STENT SYSTEM, MODELS 1010102-38,1010102-56,1010102-80,1010103-38,1010103-56, 101010
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ALGINOR ALGINELLE TYPE 1 AND 2 MILLENIUM KROMOPAN 1 AND 2
FDA 510(k)
FDA Class 2
·Dental
UNK
FDA Adverse Event
Other
·I-FLOW CORP.·Product code MEB·November 4, 2008
COBALT CHROME CABLE/SLEEVE SET 2.0MM DIA. X 750MM LGTH.
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JDQ·August 24, 2011
UNIVERSAL BLOCK TRAY
FDA Adverse Event
Malfunction
·INTEGRA PAIN MANAGEMENT·Product code FMF·July 3, 2013