565 results · 21ms · 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.

Amvex Vacuum Regulator

FDA UDI
OHIO MEDICAL, LLC·00628101501556·VR-PP series, VacReg, Ped Int 2Mode 160mmHg, A...

Actua Knee Pneumatic

FDA UDI
CYPRESS ADAPTIVE, LLC·00850013242313·The Actua Knee is a polycentric pneumatic knee ...

NOVAE

FDA UDI
SOC ETUDES RECHERCHES FABRICATION·03662200013401·

Cook

FDA UDI
COOK INCORPORATED·00827002478589·Cook, Disposable Biopsy Needle And Periprostati...

Cook

FDA UDI
COOK INCORPORATED·00827002478596·Cook, Disposable Biopsy Needle And Periprostati...

ALARIS® PUMP MODULE ADMINISTRATION SET

FDA Adverse Event
Malfunction ·CAREFUSION·Product code FPA·February 28, 2019

PRIMARY PLUM SET, 1.2 MICRON FILTER, CLAVE Y-SITE, SECURE LOCK, 104 INCH

FDA Adverse Event
Malfunction ·ICU MEDICAL COSTA RICA LTD.·Product code FPA·October 29, 2025

LIPID FILTER, 1.2 MICRON

FDA Adverse Event
Malfunction ·CODAN MEDLON, INC.·Product code FPD·May 24, 1994

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009

ACTIVA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 30, 2012

IMPLANTED SUBCORTICAL ELECTRICAL STIMULATOR (MOTOR DISORDERS)

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MRU·May 11, 2016

SET, ADMINISTRATION, INTRAVASCULAR

FDA Adverse Event
Malfunction ·Product code FPA·February 21, 2019

PPN IV TUBING

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·January 7, 2026

1 Ppn Uni 45cm

FDA UDI
Surgical Specialties México, S. de R.L. de C.V.·00848782020560·1 Ppn Uni 45cm

0 Ppn Uni 30cm

FDA UDI
Surgical Specialties México, S. de R.L. de C.V.·00848782020553·0 Ppn Uni 30cm

2 Ppn Uni 45cm

FDA UDI
Surgical Specialties México, S. de R.L. de C.V.·00848782020577·2 Ppn Uni 45cm

UNKNOWN DEEP BRAIN STIMULATOR

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 12, 2010

PLUM XLM SINGLE CHAN

FDA Adverse Event
Malfunction ·ABBOTT LABORATORIES·Product code FRN·October 6, 2000

SOLETRA

FDA Adverse Event
Injury ·MEDTRONIC NEUROMODULATION·Product code MHY·April 12, 2010

QUILL SRS

FDA Adverse Event
Other ·SURGICAL SPECIALTIES CORPORATION (DBA ANGIOTECH)·Product code NEW·May 12, 2009