28 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAPILLARYS HEMOGLOBIN, CAPILLARYS FLEX PIERCING SYSTEM
FDA 510(k)
FDA Class 2
·Hematology
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169605305·SPACER 2112550 OLIF25 20MM 12 DEG 16X50
N/A
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00721902167515·REAMER 9112550 ADJ 20MM CYLNIDER
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00763000035747·BUR 3112550 CROSSCUT TAPER SIDE CUT
N/A
FDA UDI
MEDTRONIC XOMED, INC.·00681490068567·BUR 3112550 CROSSCUT TAPER SIDE CUT
B.BRAUN
FDA UDI
B. BRAUN MEDICAL INC.·04046964656101·Transfer Set - 26 Lines
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04250317320513·
METZENBAUM SCISSORS
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896075504·METZENBAUM SCISSORS CURVED TUNGSTEN CARBIDE SER...
Unity
FDA UDI
DIOMEDICAL CO.,LTD.·08800039821339·SIJ Standard Thread OD12.5xL50
UNIMAX
FDA UDI
PARAMOUNT SURGICALS, INC.·00852647007221·HORIZONTAL PLATE STANDARD 55 MM
SONOMA FASTRAC CLAVICLE FRACTURE REPAIR DEVICE MODEL SONOMA FASTRAC XXYYY(X=DIA, YYY=LENGTH- IN MM)
FDA 510(k)
FDA Class 2
·Orthopedic
BRIGHT EMBRACE MODEL SBL60
FDA 510(k)
FDA Class 2
·General Hospital
Experience
FDA UDI
Gc Orthodontics America Inc.·D78811255000201·EXC MBT 022/U5 UNIV -7T 0A
Experience
FDA UDI
Gc Orthodontics America Inc.·E53511255000201·EXC MBT 022/U5 UNIV -7T 0A
LONG NAIL KIT R2.0, TI, RIGHT GAMMA3 Ø11X380MM X 125°
FDA Adverse Event
Injury
·STRYKER OSTEOSYNTHESIS-KIEL·Product code HSB·April 12, 2013
THERMOCOOL® SMART TOUCH® SF BI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Injury
·BIOSENSE WEBSTER INC·Product code LPB·June 6, 2018
MAXICIDE PLUS 3.4% GLUTARALDEHYDE
FDA Adverse Event
Injury
·METREX RESEARCH·Product code MED·May 14, 2013
NON AC-POWERED PATIENT LIFT
FDA Adverse Event
Malfunction
·UNKNOWN·Product code FSA·September 24, 2014
ZOOM CRITICAL CARE BED
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·May 25, 2011
26-Lead Transfer Set for use with APEX Compounding System, Product Catalog Number 2112550
FDA Recall
Terminated
·B. Braun Medical, Inc.·Product code NEP·June 4, 2018