26 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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FREELITE HUMAN KAPPA AND LAMBDA FREE KITS FOR USE ON THE BAYER ADVIA 1650 ANALYZER
FDA 510(k)
FDA Class 2
·Immunology
PYRAMESH® Implant System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000855758·MESH 9051915 PYRMSH IMPL 19MM AGL 10X15
PYRAMESH® Implant System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00681490484602·MESH 9051915 PYRMSH IMPL 19MM AGL 10X15
NON-BR2000 LARGE BONE BLADES
FDA UDI
Peter Brasseler Holdings, LLC·00887919095156·KM519-15
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274712·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274637·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274767·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613064283·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613066669·
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613049877·
NA
FDA UDI
STERILMED, INC.·10888551017367·SAW BLADE SAGITTAL SYNTHES REPLACEMENT
KOMET Surgical Saw Blade
FDA UDI
Gebr. Brasseler GmbH & Co. KG·14053613274835·
GRAFT MARKER RING
FDA 510(k)
FDA Class 2
·Cardiovascular
TRANSITIONAL IMPLANTS
FDA 510(k)
FDA Class 2
·Dental
CELL-DYN DILUENT/SHEATH
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 11, 2013
VENTAK PRIZM
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·April 12, 2011
SKIN SHAVER PREP RAZOR STERILE
FDA Adverse Event
Malfunction
·TYCO HEALTHCARE/KENDALL·Product code LWK·May 23, 2008
GUIDE WIRE, BALL-TIPPED, STERILE T2 HUMERUS Ø2.5X800 MM
FDA Adverse Event
Injury
·STRYKER TRAUMA KIEL·Product code LXH·April 25, 2016
OT ULTRA METER
FDA Adverse Event
Injury
·LIFESCAN INC.·Product code NBW·December 10, 2010