27 results · 39ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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