28 results · 22ms · Sources: EU EUDAMED, 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