40 results · 30ms · Sources: EU EUDAMED, US FDA

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IMPERIAL SURGICAL LTD. BLANKEY AND SOLUTION WARNING CABINETS

FDA 510(k)
FDA Class 2 ·General Hospital

HEX-FIX

FDA UDI
Smith & Nephew, Inc.·03596010042163·HEX-FIX HEX BAR MEDIUM 406MM ALUMINUM

4260

FDA UDI
HANS RUDOLPH, INC.·00874750009831·4260A MS.625FB 22/15MM

K2M General Instruments

FDA UDI
VB Spine LLC·10888857529847·Inserter, Outer Shaft/Handle

BUECHEL-PAPPAS (B-P) FIXED BEARING NEW JERSEY (NJ) TOTAL KNEE, MODEL 1

FDA 510(k)
FDA Class 2 ·Orthopedic

AMICUS SEPARATOR SYSTEM- USE IN THERAPEUTIC PLASMA EXCHANGE AND FILTER SET FOR AMICUS TPE

FDA 510(k)
FDA Unclassified ·Unknown

Alere iCup Dx Pro

FDA UDI
Instant Technologies, Inc.·00817405020317·Urine Drug Screening Device for detection of Am...

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

XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code NIQ·May 14, 2013

REPLY

FDA Adverse Event
Injury ·SORIN GROUP ITALIA S.R.L. - CRM FACILITY·Product code NVZ·September 24, 2014