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Crédits
Manufacturers
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Adresse du fabricant
Abbott Vascular-Cardiac Therapies dba Guidant Corporation, 26531 Ynez Rd, Temecula CA 92591-4630
Source
USFDA
17 Events
Rappel de Device Recall ACS
Rappel de Device Recall DUOSTAT
Rappel de Device Recall ACS
Rappel de Device Recall Guidant MultiLink RX Vision
Rappel de Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape ALR 1.2
Rappel de Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape BPL
Rappel de Device Recall VOYAGER NC Coronary Dilatation Catheter
Rappel de Device Recall VOYAGER NC Coronary Dilatation Catheter
Rappel de Device Recall StarClose
Rappel de Device Recall POWERSAIL
Rappel de Device Recall POWERSAIL
Rappel de Device Recall POWERSAIL
Rappel de Device Recall POWERSAIL
Rappel de Device Recall XACT Carotid Stent System
Rappel de Device Recall Viatrac 14 Plus Peripheral Dilatation Catheter
Rappel de Device Recall XACT Carotid Stent System
Rappel de Device Recall RX ACCULINK Carotid Stent System
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17 dispositifs dans la base de données
Device Recall ACS
Modèle / numéro de série
6090751, 6090752, 6091151, 6091152
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Description du dispositif
ACS Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 23242
Device Recall DUOSTAT
Modèle / numéro de série
6090551
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Description du dispositif
ACS DUOSTAT¿ Rotating Hemostatic Valve, 0.096 inch, for use with a dilatation catheter - Reference Number 23244
Device Recall ACS
Modèle / numéro de série
6090651, 6090652 , 6090653
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Worldwide, including USA, Canada, Germany, Italy, Greece, New Zealand, Netherlands, France, Japan, Spain, and Bulgaria.
Description du dispositif
ACS Rotating Hemostatic Valve, .115 inch, for use with a dilatation catheter - Reference Number 23245
Device Recall Guidant MultiLink RX Vision
Modèle / numéro de série
Part number 1007848-15, lot number 7052951
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Nationwide
Description du dispositif
Multi-Link Vision RX Coronary Stent System, 3.0 x 15mm, Part number 1007848-15, lot number 7052951
Device Recall Abbott Vascular 6F Viking Guiding Catheter, Shape ALR 1.2
Modèle / numéro de série
Lot Number: 8011791
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide Distribution.
Description du dispositif
6F Viking Guiding Catheter, Percutaneous catheter, Shape ALR 1.2, Part Number: 1001934-06, Abbott Vascular, Santa Clara, CA 95054. || Designed to provide a pathway trough which therapeutic and diagnostic devices are introduced.
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