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

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MICROBLADE SHAVER AND ACCESSORIES

FDA 510(k)
FDA Class 2 ·Neurology

ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

FDA UDI
FX SOLUTIONS·03701037314975·Ø32 Eccentric Glenosphere with +3mm lateralized...

HMS NEUROMUSCULAR STIMULATOR, MODEL HMS 3

FDA 510(k)
FDA Class 2 ·Neurology

AVID-NIT PLASTIC HUB LUTZ EPIDURAL NEEDLE,MODEL RP2035L, AVID-NIT METAL HUB LUTZ EPIDURAL NEEDLE, MODEL RM2035L

FDA 510(k)
FDA Class 2 ·Anesthesiology

MICROBORE EXT SET

FDA Adverse Event
Malfunction ·HOSPIRA LTD.·Product code FPA·February 5, 2009

SOLUSET 100 BURETTE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·May 1, 2009

SOLUSET 100X60 CE-SL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009

SOLUSET 100X60 CE-SL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009

SOLUSET 150 BURETTE

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·March 12, 2009

SOLUSET 100X60 CE-SL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009

SOLUSET 100X60 CE-SL

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·June 18, 2009

SVENTED IV PUMPSET/C

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 20, 2009

EXTENSION SET WITH T-CONNECTOR (500/CS)

FDA Adverse Event
Malfunction ·HOSPIRA LTD.·Product code FPA·March 25, 2010

EXTENSION SET WITH T-CONNECTOR (500/CS)

FDA Adverse Event
Malfunction ·HOSPIRA, LTD.·Product code FPA·March 25, 2010

EXTENSION SET WITH T-CONNECTOR (500/CS)

FDA Adverse Event
Malfunction ·HOSPIRA, LTD·Product code FPK·May 3, 2010

EXTENSION SET WITH T-CONNECTOR(500/CS)

FDA Adverse Event
Malfunction ·HOSPIRA, LTD.·Product code FPA·December 16, 2009

NV FIL SOLUSET 100

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA·Product code FPA·December 27, 2011

SOLUSET 100X60W/ CAI

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 19, 2013

NV FIL SOLUSET 100

FDA Adverse Event
Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 22, 2010

R SERIES DEFIBRILLATOR

FDA Adverse Event
Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·February 26, 2013