9 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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DIGENE CERVICAL BRUSH
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994580764·GUIDE 6971586 TRIAL CUTTER GUIDE 6X18
Brasseler
FDA UDI
Provision·B504OMKM715860·
BIORAPTOR 2.3 PK SUTURE ANCHOR
FDA 510(k)
FDA Class 2
·Orthopedic
Smart External Drain (SED) System
FDA 510(k)
FDA Class 2
·Neurology
DWF CATHETER, CANNULA AND TUBING, VASCULAR, CARDIOPULMONARY BYPASS
FDA Adverse Event
Injury
·COOK VASCULAR INC·Product code DWF·December 15, 2016
ALTRX NEUT 36IDX54OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS INC US·Product code LPH·February 21, 2013
COLLEAGUE CXE VOLUMETRICINFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·January 27, 2011
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·INVACARE REHABILITATION EQUIP·Product code FSA·July 31, 2014