194 results · 24ms · Sources: EU EUDAMED, US FDA

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COTTONY II, SILKY II POLYDEK & TEVDEK II POLYESTER SUTURE

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

ROLLO 210X30X12E.PRINTER

FDA UDI
AB MEDICA GROUP, S.A.·08428763005704·

Humeris Shoulder

FDA UDI
FX SOLUTIONS·03701037304556·TRIAL HUMERIS STEM T19

740 SELECT

FDA UDI
ZOE MEDICAL INCORPORATED·00851920007248·The 740 SELECT Monitor is intended for monitori...

COLOR BUFFED (CB) DDH FEMORAL STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

TI500 GLOBE-TROTTER TRANSPORT SYSTEM

FDA 510(k)
FDA Class 2 ·General Hospital

POLARCATH

FDA Adverse Event
Injury ·BOSTON SCIENTIFIC - SAN JOSE·Product code DQY·March 26, 2013

ATTAIN OTW

FDA Adverse Event
Death ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·March 16, 2011

GE OEC 8800

FDA Adverse Event
Malfunction ·GE OEC MEDICAL SYSTEM INC.·Product code JAA·March 28, 2008

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·November 11, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 23, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·May 9, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 18, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 16, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·April 2, 2012

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN, INC.·Product code NBW·October 5, 2010

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·January 10, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·February 17, 2011

OT ULTRASMART METER

FDA Adverse Event
Injury ·LIFESCAN INC.·Product code NBW·March 2, 2011