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

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S.I.N. Instrument Kits

FDA 510(k)
FDA Class 2 ·General Hospital

DJO SURGICAL

FDA UDI
Encore Medical, L.P.·00190446834120·SPECIAL, 21MM - 23MM SPACER BLOCK

HHM

FDA UDI
Oticon A/S·05707131357403·G300 SC, MINIRITE R LI-ION 2.4G C094 HHM

CODMAN

FDA UDI
Cerenovus, Inc.·10886704066798·CODMAN SLIM-LINE Aneurysm Clip Straight Blade L...

NA

FDA UDI
Synthes GmbH·10886982142542·2.4MM CORTEX SCREW 3.5MM HEAD/SELF-TAPPING 36MM

DATEX-OHMEDA TUFFSAT 3000 PULSE OXIMETER

FDA 510(k)
FDA Class 2 ·Cardiovascular

NICALERT

FDA 510(k)
FDA Class 1 ·Clinical Toxicology

ETHILON NYLON SUTURE UNKNOWN PRODUCT

FDA Adverse Event
Injury ·ETHICON INC.·Product code GAR·December 7, 2018

TENDRIL STS

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CRMD·Product code DTB·January 13, 2014

VBEAM

FDA Adverse Event
Injury ·CANDELA CORPORATION·Product code GEX·June 28, 2013

SPRINT QUATTRO SECURE

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 11, 2011

HAMILTON-C6

FDA Adverse Event
Malfunction ·HAMILTON MEDICAL AG·Product code CBK·February 10, 2025

MELODY TRANSCATHER PULMONARY VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPV·February 16, 2017

FREESTYLE AORTIC ROOT BIOPROSTHESIS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 6, 2016

SPRINT QUATTRO SECURE S

FDA Adverse Event
Malfunction ·MPRI·Product code LWS·August 9, 2016

FREESTYLE AORTIC ROOT BIOPROSTHESIS

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·December 7, 2016

COREVALVE TRANSCATHETER AORTIC VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code NPT·September 29, 2017

UNK - SCREWS: PHILOS

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 9, 2021

UNK - CONSTRUCTS: PHILOS PLATE/SCREWS

FDA Adverse Event
Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HRS·June 9, 2021

MOSAIC MITRAL BIOPROSTHETIC HEART VALVE

FDA Adverse Event
Injury ·MEDTRONIC HEART VALVES DIVISION·Product code LWR·September 28, 2016