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

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

2915056-1998-00003

FDA Adverse Event
Malfunction ·Product code KOD·October 22, 1998

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

RAPIDSTRAND RX

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011

IODINE (I-125) SEEDS

FDA Adverse Event
Malfunction ·GE HEALTHCARE·Product code KXK·September 26, 2011