27 results
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39ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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BIOCARDIA, INC.
FDA registration
BIOCARDIA, INC.·3 products·🇺🇸 United States
Morph AccessPro Steerable Introducer
FDA UDI
BIOCARDIA, INC.·00866749000240·
Morph AccessPro Steerable Introducer
FDA UDI
BIOCARDIA, INC.·00866749000257·
Avance Steerable Introducer
FDA UDI
Biocardia, Inc.·00850007221003·Cardiovascular catheter introducer
Avance Steerable Catheter
FDA UDI
Biocardia, Inc.·00850007221027·Cardiovascular catheter introducer
Helical Infusion Catheter
FDA UDI
Biocardia, Inc.·00866749000271·Catheter, percutaneous
Avance Steerable Introducer
FDA UDI
Biocardia, Inc.·00850007221010·Cardiovascular Catheter introducer
Morph DNA
FDA UDI
Biocardia, Inc.·00866749000295·Guide Catheter
Morph Universal Deflectable Guide Catheter
FDA UDI
BIOCARDIA, INC.·00866749000202·
BIOCARDIA MORPH ACCESSPRO STEERABLE INTRODUCER
FDA Adverse Event
Malfunction
·BIOCARDIA, INC.·Product code DYB·July 26, 2013
BIOCARDIA MORPH SHEATH GUIDE
FDA 510(k)
FDA Class 2
·Cardiovascular
BIOCARDIA MORPH UNIVERSAL DEFLECTABLE GUIDE CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
BioCardia 8.5 F Avance Steerable lntroducer
FDA 510(k)
FDA Class 2
·Cardiovascular
MORPH UNIVERSAL DEFLECTABLE GUIDE CATHETER
FDA Adverse Event
Injury
·BIOCARDIA, INC.·Product code DQY·February 17, 2015
BIOCARDIA MORPH ACCESSPRO
FDA Adverse Event
Injury
·BIOCARDIA, INC.·Product code DYB·June 14, 2012
BIOCARDIA UNIVERSAL DEFLECTABLE GUIDE CATHETER, MODEL 000664
FDA 510(k)
FDA Class 2
·Cardiovascular
BioCardia 8F Morph DNA Deflectable Guide Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
MORPH ACCESSPRO STEERABLE INTRODUCER
FDA Adverse Event
Malfunction
·BIOCARDIA·Product code DYB·June 19, 2013
BIOCARDIA MORPH UNIVERSAL DEFLECTABLE GUIDE 6F
FDA Adverse Event
Injury
·BIOCARDIA, INC.·Product code DQY·March 25, 2010
BIOCARDIA MORPH UNIVERSAL DEFLECTABLE GUIDE
FDA Adverse Event
Injury
·BIOCARDIA, INC.·Product code DQX·October 30, 2009