10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIOSTRIP(R) HCG-ONE STEP PREGNANCY TEST
FDA 510(k)
FDA Class 2
·Clinical Chemistry
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04064984699595·GENUMEDI PSS BLUE, SIZE VII
BASE
FDA UDI
Nuvasive, Inc.·00887517700452·BASE Guide, G
AIRIS ELITE RAPID BODY COIL
FDA 510(k)
FDA Class 2
·Radiology
RESTORIS Multicompartmental Knee System
FDA 510(k)
FDA Class 2
·Orthopedic
BD ANGIOCATH¿ IV CATHETER 22 G X 1"
FDA Adverse Event
Malfunction
·BECTON DICKINSON INDUSTRIAS CIRURGICAS, LTDA.·Product code FOZ·September 13, 2017
EON MINI
FDA Adverse Event
Injury
·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·June 19, 2014
ELITE & USA DISPOSABLE ACTIVE CORD
FDA Adverse Event
Injury
·GYRUS MEDICAL, INC.·Product code HIH·February 6, 2013
ACCURUS 800CS
FDA Adverse Event
Malfunction
·ALCON - IRVINE TECHNOLOGY CENTER·Product code HQC·December 14, 2010
BD ANGIOCATH¿ IV CATHETER
FDA Adverse Event
Malfunction
·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FOZ·August 8, 2017