28 results · 42ms · 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.

TRIDENT ALL POLY CUP

FDA 510(k)
FDA Class 2 ·Orthopedic

LIFEPAK® 15 monitor/defibrillator

FDA UDI
PHYSIO-CONTROL, INC.·00883873871706·15AABBABBABBBBAAAAAAAAAFLP15 MONITOR/DEFIB

OLYMPIC WARM-UP

FDA 510(k)
FDA Class 2 ·Physical Medicine

MODIFICATION TO SCIMED 6F IMPULSE ANGIOGRAPHIC CATHATERS

FDA 510(k)
FDA Class 2 ·Cardiovascular

9616240-2006-00341

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

9616240-2006-00332

FDA Adverse Event
Other ·Product code FII·June 1, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

9616240-2006-00339

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00340

FDA Adverse Event
Malfunction ·Product code FII·June 9, 2006

9616240-2006-00350

FDA Adverse Event
Malfunction ·Product code FII·June 23, 2006

9616240-2006-00345

FDA Adverse Event
Malfunction ·Product code FII·June 14, 2006

VENTAK MINI+

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·August 5, 1998

ENDOTAK C

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·May 5, 1998

SUBCUTANEOUS PATCH

FDA Adverse Event
Malfunction ·CARDIAC PACEMAKERS·Product code LWS·May 5, 1998

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

PHOENIX

FDA Adverse Event
Malfunction ·GAMBRO DASCO·Product code FII·May 10, 2006

PUMP IN STYLE ADVANCED BREAST PUMP GO TOTE

FDA Adverse Event
Malfunction ·MEDELA, INC.·Product code HGX·March 11, 2013

PRECISION XTRA

FDA Adverse Event
Malfunction ·Product code NBW·February 27, 2011

EDGE INSUL COATED NEEDLE

FDA Adverse Event
Injury ·COVIDIEN LP (VALLEYLAB)·Product code GEI·February 20, 2008

TECNIS SIMPLICITY

FDA Adverse Event
Injury ·AMO PUERTO RICO MFG. INC.·Product code HQL·July 16, 2025