34 results · 22ms · 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.

SYSTEMS INTEGRATION

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04049772813148·GENUMEDI PRO SILVER SIZE I

ICU Medical

FDA UDI
ICU MEDICAL, INC.·00840619043988·TD Catheter, 8F, 5 lumen, 110 cm, RA/RA

Cardiovascular Procedure Kit

FDA UDI
Terumo Cardiovascular Systems Corporation·00699753464247·

eTRAX™ Needle

FDA UDI
CIVCO MEDICAL INSTRUMENTS CO., INC.·00841436102520·Sterile needle, 12GA x 17cm with (7.6 tapered t...

CHARGER BALLOON DILATATION CATHETER

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

SURGASSIST RIGHT ANGLE LINEAR CUTTER 30MM, 45MM & 60MM, MODELS RALC30, RALC45 & RALC60

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

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 17, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 24, 2024

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 21, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·June 2, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 11, 2024

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·March 27, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·December 10, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·November 17, 2025

CHARGER?

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·August 6, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·February 6, 2025

CHARGER

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code FGE·March 25, 2025

MAXI MOVE

FDA Adverse Event
Malfunction ·ARJOHUNTLEIGH MAGOG INC·Product code FSA·May 9, 2013

PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

FDA Adverse Event
Malfunction ·INVACARE TAYLOR STREET·Product code CAW·September 26, 2014