19 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SUB-TALAR LOK, MODEL 7-11 MM
FDA 510(k)
FDA Class 2
·Orthopedic
AORTIC ROOT RETRACTOR
FDA UDI
LSI Solutions, Inc.·00850200006568·AORTIC ROOT RETRACTOR, LARGE
SchureMed
FDA UDI
SCHUERCH CORPORATION·00810014605524·MAQUET 1130 ORTHOPEDIC 2.25" DELUXE GEL
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450180594·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450182840·
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450169636·
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197500685·VATS MICS Chest Tube Passer
WL 280...
PRECINORM PROTEINS IN URINE/CSF PRECIPATH PROTEINS IN URINE/CSR CONTROLS
FDA 510(k)
FDA Class 1
·Clinical Chemistry
PULMOLAB EX671 EXERCISE TESTING SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology
NEURAGEN NERVE GUIDE 2MM ID X 2CM LENGTH
FDA Adverse Event
Other
·INTEGRA LIFESCIENCES CORP.·Product code JXI·June 14, 2010
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·April 30, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·August 24, 2009
ALIGN URETHRAL SUPPORT SYSTEM
FDA Adverse Event
Injury
·C.R. BARD, INC. (COVINGTON) -1018233·Product code OTN·April 24, 2013
INRATIO
FDA Adverse Event
Malfunction
·ALERE SAN DIEGO, INC.·Product code GJS·March 31, 2011
SYNERGY
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO·Product code LGW·July 22, 2008
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·March 12, 2009
QUILL SRS
FDA Adverse Event
Other
·SURGICAL SPECIALTIES CORP. (DBA ANGIOTECH)·Product code NEW·October 31, 2008
On-Board Imager - Exact Arm Elbow Motor Shaft (kVD, kVS, and MV) with ''Type 01" elbow motors. Product Usage: The On-Board Imager device is an x-ray device used for evaluation of correct patient position in relation to isocenter and verification of treatment fields in relation to anatomical and fiducial landmarks.
FDA Enforcement
Class II
·Terminated·Varian Medical Systems, Inc.·April 30, 2014