29 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NuStat
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
OsteoMed
FDA UDI
OSTEOMED LLC·00842528123300·SmartFlex Spring NC- 9.0N
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197032308·Potts-Smith Vascular Scissors
60° an...
RZ Medizintechnik GmbH
FDA UDI
RZ-Medizintechnik GmbH·04049197039789·Super-Cut Potts-Smith Vascular Scissors
25° an...
LEAD
FDA Adverse Event
Injury
·NEUROLOGICAL DIV, METRONIC, INC.·Product code LGW·March 19, 2007
RESUME II OR RESUME TL
FDA Adverse Event
Injury
·MEDTRONIC, INC. NEUROLOGICAL DIVISION·Product code GZB·March 23, 2007
D-STAT DRY WRAP HEMOSTATIC BANDAGE, MODEL: 3015
FDA 510(k)
FDA Unclassified
·Unknown
PROFIL COMPOSITES (PROFIL, PROFIL FLOW)
FDA 510(k)
FDA Class 2
·Dental
LEAD
FDA Adverse Event
Injury
·MEDTRONIC, INC., NEUROLOGICAL DIVISION·Product code LGW·March 19, 2007
SPECIFY
FDA Adverse Event
Injury
·MEDTRONIC NEUROLOGICAL·Product code GZB·March 19, 2007
ONE TOUCH BASIC ENHANCED
FDA Adverse Event
Malfunction
·LIFESCAN, INC.·Product code CFR·May 22, 2002
LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROLOGICAL·Product code LGW·March 19, 2007
LEAD
FDA Adverse Event
Injury
·MEDTRONIC IND, NEUROLOGICAL DIVISION·Product code LGW·March 19, 2007
RESUME II OR RESUME TL
FDA Adverse Event
Injury
·MEDTRONIC, INC., NEUROLOGICAL DIVISION·Product code GZB·March 19, 2007
GMK-REVISION 02.07.0312SCF FIXED TIBIAL INSERT SC SIZE 3/12MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·December 29, 2022
GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/12MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·October 2, 2019
GMK-REVISION FIXED TIBIAL INSERT SC SIZE 3/12MM
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JWH·June 23, 2023
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC MINIMED·Product code OYC·October 17, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 28, 2011
HOMECHOICE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - LARGO·Product code FKX·June 21, 2013