18 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ELECSYS LH CALCHECK 5
FDA 510(k)
FDA Class 1
·Clinical Chemistry
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943000054·
ArgenZ Anterior 95x20 #1
FDA UDI
ARGEN CORPORATION, THE·D818121279·Dental porcelain/ceramic restoration kit
CRYO.S
FDA UDI
Greiner Bio - One GmbH·14039943001716·
ELMED
FDA UDI
ELMED INCORPORATED·00842180161085·PRISM CERVICAL CURETTE 10" ANGLED 1, ORANGE
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970423·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970393·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970416·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970409·
DATEX-OHMEDA S/5 ANESTHESIA MONITOR WITH L-ANE02 AND L-ANE02A SOFTWARE
FDA 510(k)
FDA Class 2
·Cardiovascular
CORRIDOR4DM V2010 MODEL: V2010
FDA 510(k)
FDA Class 2
·Radiology
OT ULTRALINK METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 13, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 20, 2013
ALLEGRETTO WAVE EYE-Q
FDA Adverse Event
Injury
·WAVELIGHT GMBH·Product code LZS·September 22, 2014
CODEMASTER XL
FDA Adverse Event
Malfunction
·AGILENT TECHNOLOGIES, INC.·Product code LDD·May 4, 2011
UNKNOWN
FDA Adverse Event
Malfunction
·WILLIAM COOK EUROPE·Product code DTK·December 2, 2015
ONYX
FDA Adverse Event
Injury
·MICRO THERAPEUTICS, INC. DBA EV3·Product code MFE·July 12, 2023
Eversense CGM SENSOR (FG-4200-00-301)-Continuous Glucose Monitor
FDA Enforcement
Class II
·Terminated·Senseonics, Inc.·November 6, 2019