20 results · 23ms · Sources: EU EUDAMED, US FDA

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StatStrip Xpress Glucose Hospital Meter System

FDA 510(k)
FDA Class 2 ·Clinical Chemistry

Drill Stopper for Long L16 1856

FDA UDI
ADIN DENTAL IMPLANT SYSTEMS LTD·07290105157669·

Drill Stopper for Long L16 1856

Device
EU MDR · Eu Md Class 1 ·Adin Dental Implant Systems LTD.·On the market·32 countries

Drill Stopper for Long L16 1856

Device
EU MDR · Eu Md Class 1 ·MEDIGMA BIOMEDICAL GMBH·On the market·32 countries

Drill Stopper for Long L16 1856

Device
EU MDD · Eu Md Class 1 ·MEDIGMA BIOMEDICAL GMBH·On the market·32 countries

V-2200 INFANT INCUBATOR

FDA 510(k)
FDA Class 2 ·General Hospital

ELECSYS CEA CALCHECK 5

FDA 510(k)
FDA Class 1 ·Clinical Chemistry

AESCULAP SURGICAL INSTRUMENTS

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

AESCULAP SURGICAL INSTRUMENTS

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·November 27, 2019

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929066485·Corpectomy, 16Dx18Wx56H 6°

Matrixx System

FDA UDI
NEXXT SPINE, LLC·00889929066171·Corpectomy, 16Dx18Wx56H 0°

UNKNOWN PLATE

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

UNKNOWN PLATE

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

UNKNOWN PLATE

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·April 21, 2026

PROWLER SELECT MICROCATHETERS

FDA Adverse Event
Malfunction ·CODMAN AND SHURTLEFF, INC·Product code KRA·October 10, 2014

RSP SHOULDER

FDA Adverse Event
Other ·ENCORE MEDICAL, L.P.·Product code KWS·June 6, 2013

PULSE GEN MODEL 102

FDA Adverse Event
Injury ·CYBERONICS, INC.·Product code LYJ·July 8, 2011

STERNALOCK BLU SYSTEM BLADE, STERNALOCK POWERDRIVER

FDA Adverse Event
Malfunction ·BIOMET MICROFIXATION·Product code HRS·January 10, 2019

PROGAV SYS PED.W/SA 15 A.PRECHAMBER

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·April 4, 2019

PROGAV 2.0 SYS PED.W/SA15 A.PRECHAMBER

FDA Adverse Event
Injury ·CHRISTOPH MIETHKE GMBH & CO. KG·Product code JXG·August 6, 2020