1,123 results · 30ms · Sources: EU EUDAMED, US FDA

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CMS-1000FM CENTRAL MONITORING SYSTEM

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

DD tempMED

FDA UDI
Dental Direkt GmbH·EDDIK112151·DD tempMED are pre-colored dental milling blank...

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089422401·

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089422432·

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089422418·

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089422425·

Surgical Instrument

FDA UDI
Jeil Medical Corporation·08800089422449·

RAPID DRUG SCREEN

FDA 510(k)
FDA Class 2 ·Clinical Toxicology

POWERPICC SV CATHETERS

FDA 510(k)
FDA Class 2 ·General Hospital

UniTip High Resolution Catheter

FDA UDI
Unisensor AG·07640172974032·UniTip High Resolution Catheter 12F

GUNTHER TULIP JUGULAR VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·January 5, 2017

LIFEVEST WCD 4000 SYSTEM

FDA Adverse Event
Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·May 3, 2013

530G INSULIN PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC MINIMED·Product code OZO·September 23, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 2, 2011

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·May 20, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·August 14, 2015

UNKNOWN

FDA Adverse Event
Malfunction ·WILLIAM COOK EUROPE·Product code DTK·March 10, 2016

GUNTHER TULIP JUGULAR & FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·February 9, 2017

GUNTHER TULIP FEMORAL VENA CAVA FILTER SET

FDA Adverse Event
Injury ·COOK INC·Product code DTK·June 3, 2016

UNKNOWN

FDA Adverse Event
Injury ·WILLIAM COOK EUROPE·Product code DTK·January 5, 2017