29 results · 25ms · Sources: EU EUDAMED, 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