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

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THE SOLOPATH BALLOON EXPANDABLE TRANSFEMORAL INTRODUCER

FDA 510(k)
FDA Class 2 ·Cardiovascular

Bur PM2-95 80K MstickD Ø3.0 St

FDA UDI
Bien-Air Surgery SA·17630055514957·

ILIZAROV

FDA UDI
Smith & Nephew, Inc.·03596010029751·2 HOLE SHORT PLATE - SMALL BONE FIXATOR

V.A.T.S. CLASSIC CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·B09921008190·V.A.T.S. CLASSIC CLAMP WITH RATCHET DEBAKEY JAW...

V.A.T.S. CLASSIC CLAMP

FDA UDI
SONTEC INSTRUMENTS, INC.·00192896003552·V.A.T.S. CLASSIC CLAMP WITH RATCHET DEBAKEY JAW...

Arena-L®

FDA UDI
SPINEFRONTIER, INC.·00190361005841·Arena-L, 38x28, Lordotic 12 degrees, 19H

CareLiving Blood Glucose Test Strips 100ct

FDA UDI
Care Living Diagnostics Inc.·00383568100819·Blood Glucose Test Strips,50ct/box,two box, for...

N/A

FDA UDI
Doppkon GmbH & Co. KG·04262494463709·Curette straight D 6mm, L 9mm, WL 120mm

PHILIPS CT SECURA MV

FDA 510(k)
FDA Class 2 ·Radiology

3CC NMT SAFETY SYRINGE

FDA 510(k)
FDA Class 2 ·General Hospital

Widex

FDA UDI
Widex A/S·05706069727265·Widex EVOKE E-FM (Summer gold S-330 ) RC coil

Widex

FDA UDI
Widex A/S·05706069727661·Widex EVOKE E-FA (Summer gold S-330 ) Telecoil,...

Widex

FDA UDI
Widex A/S·05706069729665·Widex EVOKE E-FP (Summer gold S-330 ) Telecoil,...

ADULT DUAL-HEATED BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LTD.·Product code BZE·October 18, 2010

ANIMAS INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·May 8, 2013

NAVI-STAR THERMO-COOL

FDA Adverse Event
BIOSENSE WEBSTER·Product code OAD·July 28, 2008

ECHELON*FLEX60 ARTICULATING

FDA Adverse Event
Injury ·ETHICON ENDO SURGERY, INC (CINCINNATI)·Product code GDW·May 24, 2011

VENTED AUTOFEED HUMIDIFICATION CHAMBER

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·May 12, 2011

EVOLUT FX PLUS VALVE

FDA Adverse Event
Injury ·MEDTRONIC MEXICO S. DE R.L. DE CV·Product code NPT·August 27, 2025

ADULT DUAL-HEATED EVAQUA BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BZE·April 5, 2011