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

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NIPRO BIOHOLE NEEDLE WITH CAPICK SCAB REMOVER

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

COOLEY BULLDOG CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921005200·COOLEY BULLDOG CLAMP RING HANDLE ANGLED JAW CUR...

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450186954·

HS Diam. Burr, Ø3.1x70, 50k

FDA UDI
Bien-Air Surgery SA·07630055506610·

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361005506·Arena-L, Lordotic 10 degrees, 35X26X20

NA

FDA UDI
ST. JUDE MEDICAL, INC.·05415067028228·SL Radiofrequency Cannula - Curved

NeuroTherm™

FDA UDI
NEUROTHERM, INC.·05415067021717·

GEM PREMIER 3000- ADDITION OF GLUCOSE AND LACTATE AS NEW PARAMETERS

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

C-IT

FDA 510(k)
FDA Class 2 ·Anesthesiology

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·May 8, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·September 19, 2014

TERUMO CDI 540 CALIBRATOR

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEM CORP.·Product code DRY·May 13, 2011

CAPIOX®FX

FDA Adverse Event
Death ·TERUMO CORPORATION, ASHITAKA·Product code DTZ·June 27, 2025

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 14, 2026

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 13, 2026

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 13, 2026

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 14, 2026

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 13, 2026

IRRIG CYSTOTOME FORMED .50MM (PEARCE) (10/SP)

FDA Adverse Event
Malfunction ·BEAVER-VISITEC INTERNATIONAL, INC.·Product code HNY·May 13, 2026

BD NEXIVA¿ CLOSED IV CATHETER SYSTEM

FDA Adverse Event
Malfunction ·Product code FOZ·June 25, 2021