41 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ACCUCORE SINGLE ACTION CORE BIOPSY DEVICE
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PowerPICC SOLO
FDA UDI
Bard Access Systems, Inc.·00801741121388·Catheter Placement Kit
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317302151·
N/A
FDA UDI
Ortho Development Corporation·00822409090419·Alpine Reamer Size 12
Tooth Tone
FDA UDI
ORTHO TECHNOLOGY, INC.·00190730014856·NiTi Coated Upper 20x20 10 archwires per pack
LEGION
FDA UDI
Smith & Nephew, Inc.·00885556693117·LEGION TRIAL STEM 17 X 160MM
LEGION
FDA UDI
Smith & Nephew, Inc.·00885556693124·LEGION REAMER 17MM
LEGION
FDA UDI
Smith & Nephew, Inc.·00885556693100·LEGION PRESSFIT STEM 17MM X 160MM
ER9W CDMA wEvent
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ER9WCNC0·
ER9W AMI
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ERWCD060·
ER9W Cardiomedix
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ERWCD050·
ER9W CDMA First Call Med
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ERWCD020·
ER9W Cardiolabs
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ERWCD040·
ER9W CDMA UNM
FDA UDI
BRAEMAR MANUFACTURING, LLC·B146ERWCD030·
APPLIANCE, FIXATION, NAIL
FDA Adverse Event
Injury
·SYNTHES USA·Product code KTT·August 18, 2015
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES USA·Product code HWC·January 5, 2016
IMMULITE PHENOBARBITAL, MODELS LKPB1, LKPB5
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ACUCAM CONCEPT IV, MODELS A1222B, A1223B, A1221B, A1121B, A1222C, A10402, A10403, A10401
FDA 510(k)
FDA Class 1
·Dental
TUFF-TT IMPLANT
FDA Adverse Event
Injury
·NORIS MEDICAL LTD·Product code DZE·May 15, 2024
SCREW, FIXATION, BONE
FDA Adverse Event
Injury
·SYNTHES BETTLACH·Product code HWC·September 23, 2015