33 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HEMO-Bandage
FDA 510(k)
FDA Unclassified
·Unknown
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04049772813841·GENUMEDI PRO SILVER SIZE IV
LinkSymphoKnee
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575289820·Tibial Cutting Block, right
BD PHOENIX AUTOMATED MICROBIOLOGY SYSTEM CEFEPIME (STREP) 0.0625-4UG/ML
FDA 510(k)
FDA Class 2
·Microbiology
MEG-2 BLOOD GLUCOSE MONITORING SYSTEM, MEG-2 50'S TEST STRIP, MEG-2 CONTROL SOLUTION
FDA 510(k)
FDA Class 2
·Clinical Chemistry
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007754·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·February 13, 2026
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007808·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007778·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007785·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007761·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
VACUTRON
FDA UDI
Allied Medical, LLC·00026072007792·CONTINUOUS / INTERMITTENT SUCTION REGULATORS
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·June 26, 2024
OT PING METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 6, 2013
UNKNOWN DEPUY 36 + 1.5 HEAD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code KWY·June 30, 2011
DAMON COPPER NITI WIRE
FDA Adverse Event
Malfunction
·ORMCO CORPORATION·Product code DZC·September 9, 2008
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·October 16, 2024
BD PHOENIX¿ SMIC/ID-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 1, 2024
ADVANCE 35 LP LOW PROFILE BALLOON CATHETER
FDA Adverse Event
Malfunction
·COOK INC·Product code DQY·February 3, 2017
BD PHOENIX¿ SMIC-101
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·July 28, 2025