21 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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TM ARDIS INTERBODY SYSTEM INSERTER
FDA 510(k)
FDA Class 2
·Orthopedic
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970782·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172971192·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172973264·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970751·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970775·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970768·
N.A.
FDA UDI
DENTAURUM GmbH & Co.KG·J011123602000·Hard metal burs, drilltoothed, straight, Form: ...
EUDERMIC MP LATEX EXAMINATION GLOVE-BLUE (TESTED FOR USE WITH CHEMOTHERAPY DRUGS) W/ A PROTEIN CONTENT LABEL CLAIM
FDA 510(k)
FDA Class 1
·General Hospital
SMALL VOLUME NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·November 18, 2014
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 23, 2024
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 31, 2026
INION OTPS BIOABSOBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·May 14, 2015
WAGENER EAR HOOK, 2.5 X150
FDA Adverse Event
Malfunction
·GYRUS ACMI INC.·Product code LRC·July 24, 2015
INION OTPS BIOABSORBABLE FREEDOMPLATE
FDA Adverse Event
Injury
·INION OY·Product code HRS·March 19, 2015
OCTRODE
FDA Adverse Event
Injury
·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·May 17, 2013
INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC MINIMED·Product code OYC·September 26, 2014
MINICAP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - CALI·Product code KDI·June 14, 2011
RECAP CEMENT FMRL HD RESUR46MM
FDA Adverse Event
Injury
·BIOMET UK LTD.·Product code KWA·December 4, 2017