35 results · 24ms · Sources: EU EUDAMED, US FDA

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Exactech Equinoxe Reverse Shoulder 46x21mm Glenosphere

FDA 510(k)
FDA Class 2 ·Orthopedic

ECG Module(AHA)

FDA UDI
SAMSUNG MEDISON CO., LTD.·08806167712532·

OSS™ Orthopedic Salvage System

FDA UDI
Biomet Orthopedics, LLC·00880304239791·

AGXO

FDA UDI
Oticon A/S·05707131289032·H110V2 TI, RITE 312 WL CNB AGXO

Ophthalmic Speculum

FDA UDI
KATENA PRODUCTS, INC.·00841668100134·KRATZ-BARRAQUER SPECULUM LEFT EYE

Femoral Cutting Block Size 3

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215074388·

SILVER ANTIMICROBIAL WOUND GEL

FDA 510(k)
FDA Unclassified ·Unknown

TSX-201A AQUILION LB CT SCANNER

FDA 510(k)
FDA Class 2 ·Radiology

ADVANTAGE SYSTEM

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 6, 2013

SYNCHRON LX 20 PRO SYSTEM

FDA Adverse Event
Malfunction ·BECKMAN COULTER, INC.·Product code JGS·June 8, 2011

GE OEC 9900

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEMS INC.·Product code JAA·September 9, 2008

LINER: MPACT FLAT PE HC LINER Ø36/F

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LPH·October 19, 2018

OSS POLYETHYLENE LOCKING PIN

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS POLYETHYLENE TIBIAL BUSHING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS TIBIAL POLYETHYLENE BEARING

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018

OSS REINFORCED YOKE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code KRO·April 26, 2018

OSS POROUS IM STEM 14.5 X 150

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 11, 2021

OSS POROUS IM STEM 14.5 X 150

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 15, 2021

OSS POROUS IM STEM 14.5 X 150

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·February 11, 2021

OSS LONG TIBIAL PLATE

FDA Adverse Event
Injury ·ZIMMER BIOMET, INC.·Product code JDI·April 26, 2018