33 results · 28ms · Sources: EU EUDAMED, US FDA

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CARDIO MED

FDA 510(k)
FDA Class 2 ·Cardiovascular

Punch

FDA UDI
ADLER ORTHO SPA·08053617185228·PUNCH FOR TIBIA MB GENUS PANTHEON SZ. 3-4

ENDOFLIP

FDA 510(k)
FDA Class 2 ·Orthopedic

STICK NET

FDA 510(k)
FDA Class 2 ·Dental

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·March 21, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALUE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 21, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 9, 2012

PINNACLE MTL INS NEUT40IDX56OD

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·May 9, 2013

G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code MDS·September 19, 2014

ADVIA CENTAUR XP HBC TOTAL (HBCT)

FDA Adverse Event
SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LOM·May 26, 2011

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 14, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 5, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012

PRIM SYM SET2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·July 5, 2012

PRIM SYM SET 2 CL W/ FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 5, 2012

PRIM SYM SET 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD·Product code FPA·January 16, 2012

PRIM SYM 2 CL W/FILTERTEK VALVE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 21, 2012

PROLENE POLYPROPYLENE SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAW·February 27, 2024

VERTEBRAL DISTRACTOR

FDA Adverse Event
Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code LXH·December 10, 2018