181 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Wireless Digital Flat Panel Detector
FDA 510(k)
FDA Class 2
·Radiology
Vanguard® Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304271067·
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249295·PrimePadPlus-K15-3422
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249288·PrimePadPlus-K14-3422
Prime Medical LLC
FDA UDI
Prime Medical LLC·00850055249271·PrimePadPlus-K12-3422
Vanguard Knee System
FDA UDI
Biomet Orthopedics, LLC·00880304466111·
6F TAIGA GUIDING CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
TERUMO SURGUARD 3 SAFETY NEEDLE TERUMO SURGUARD 3 HYPODERMIC SYRINGE WITH SAFETY NEEDLE
FDA 510(k)
FDA Class 2
·General Hospital
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 22, 2013
FLOGARD
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·October 18, 2014
VANGUARD DCM CR TIBIAL BEARING 12MM X 63/67MM
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code JWH·November 8, 2016
BIOMET ILOK PRI TIB TRAY 79MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 19, 2024
VANGUARD CR ILOK FEM-RT 57.5
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 21, 2021
BIOMET CC I-BEAM TRAY 63MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 6, 2018
BIOMET CC I-BEAM TRAY 63MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·November 6, 2018
BIOMET BC R 1X40 US
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·May 25, 2026
BIOMET BC R 1X40 US
FDA Adverse Event
Injury
·BIOMET FRANCE S.A.R.L.·Product code LOD·May 25, 2026
VNGD CR INTLK FEMORAL 55MM RT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·July 8, 2020
BIOMET CC I-BEAM TRAY 67MM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·August 9, 2018