2,936 results · 25ms · Sources: EU EUDAMED, US FDA

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ARK Methotrexate II Assay

FDA 510(k)
FDA Unclassified ·Unknown

RIGIDLOOP

FDA UDI
Medos International Sàrl·10886705022687·RIGIDLOOP Cortical Fixation Implant 35mm

MEGA PLUS SPINE SYSTEM

FDA UDI
BK MEDITECH CO.,LTD.·08809665580450·Rod(CoCr), Ø5.5 x 170mm

SPEEDLOCK

FDA UDI
Smith & Nephew, Inc.·00817470002980·SPEEDLOCK HIP CORTICAL OBTURATOR

N/A

FDA UDI
ZIMMER ORTHOPAEDIC SURGICAL PRODUCTS, INC.·00889024369474·FOOT SUPPORT SMALL

HC550 RESPIRATORY HUMIDIFIER, ADULT VENTILATOR CIRCUIT

FDA 510(k)
FDA Class 2 ·Anesthesiology

LIQUICHEK D-DIMER CONTROL LEVEL 1, 2 AND 3

FDA 510(k)
FDA Class 2 ·Hematology

530G INSULIN PUMP

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

EMBOSHIELD NAV6 EMBOLIC PROTECTION SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code NTE·September 1, 2011

INSIGNIA

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NVZ·July 17, 2013

UNKNOWN

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·November 22, 2017

FLANGE FIXTURE ST 4MM W. BAHA ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·November 22, 2017

UNKNOWN

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code LXB·November 22, 2017

FLANGE FIXTURE ST 4MM W. BAHA ABUTMENT

FDA Adverse Event
Injury ·COCHLEAR BONE ANCHORED SOLUTIONS AB·Product code MAH·October 22, 2017

DEXCOM G5 MOBILE CONTINUOUS GLUCOSE MONITORING SYSTEM

FDA Adverse Event
Malfunction ·DEXCOM INC.·Product code PQF·September 14, 2017

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·April 13, 2017

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·October 16, 2017

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·October 20, 2017

ANIMAS VIBE

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code OYC·June 14, 2017

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·July 19, 2017