2,277 results · 25ms · Sources: EU EUDAMED, US FDA

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Citrated: K, KH, RTH, FFH

FDA 510(k)
FDA Class 2 ·Hematology

RIGIDLOOP

FDA UDI
Medos International Sàrl·10886705022694·RIGIDLOOP Cortical Fixation Implant 40mm

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580467·Rod(CoCr), Ø5.5 x 180mm

Sapphire NC ULTRA Coronary Dilatation Catheter

FDA UDI
OrbusNeich Medical (ShenZhen) Co., Ltd.·06934955982354·

N/A

FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369481·FOOT SUPPORT MEDIUM

SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020

FDA 510(k)
FDA Class 2 ·Orthopedic

Hill-Rom Heart and Respiration Rate Monitoring System: Single Sensor, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Packs, Hill-Rom Heart and Respiration Rate Monitoring System: Sensor Activation

FDA 510(k)
FDA Class 2 ·Anesthesiology

EASY PULSE II OXYGEN CONSERVER

FDA 510(k)
FDA Class 2 ·Anesthesiology

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·April 22, 2018

PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 6, 2014

XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·September 1, 2011

TELIGEN

FDA Adverse Event
Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·July 17, 2013

MOOG 6000 CMS

FDA Adverse Event
Malfunction ·ZEVEX INC·Product code FRN·June 26, 2017

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·March 22, 2018

TI-LOCKING SCREW, SYS3.5, HEX, 18MM

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HRS·August 7, 2018

TI-LOCKING SCREW, SYS3.5, HEX, 16MM

FDA Adverse Event
Injury ·ZIMMER GMBH·Product code HRS·August 7, 2018

HEARTWARE VENTRICULAR ASSIST SYSTEM - CONTROLLER 2.0

FDA Adverse Event
Malfunction ·HEARTWARE, INC.·Product code DSQ·June 11, 2018

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM, INC.·Product code PQF·September 20, 2018

GREENLIGHT XPS LASER SYSTEM

FDA Adverse Event
Malfunction ·AMERICAN MEDICAL SYSTEMS, INC. (SAN JOSE)·Product code GEX·February 6, 2018

HEARTSTART HOME

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code NSA·September 13, 2018