13 results
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23ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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3M Comply Lead Free Steam Indicator Tape 1322, 3M Attest Lead Free Steam Indicator Tape 1355
FDA 510(k)
FDA Class 2
·General Hospital
Medtronic Reusable Instruments
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994503398·TRASP 5220564 STAND ALONE 16X14 X 5MM
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776388072·5mm 33cm Spatula Electrode with suction/irrigat...
ELMED
FDA UDI
ELMED INCORPORATED·00842180108127·5 MM DIA., 33 CM INSULATED SPATULA ELECTRODE, T...
VEO® Lateral Interbody Fusion System
FDA UDI
Choice Spine, LP·00840996134569·LATERAL,CONVEX ENDPLATE
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197163637·CASTROVIEJO Micro Needle Holder,curved
140mm/...
EAV KINDLING 2000S GSR DEVICE
FDA 510(k)
FDA Class 2
·Neurology
CALYPSO SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
HIGHLY CROSS LINKED POLYETHYLENE LINER
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code KWB·October 31, 2008
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN INC.·Product code NBW·August 23, 2011
OT VERIO TEST STRIPS
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 11, 2013
BD CATHENA¿ SAFETY IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL (SINGAPORE)·Product code FOZ·July 7, 2022
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021