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Crédits
Devices
Device Recall Guidant
Modèle / numéro de série
Lot 4021651
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
Nationwide in the United States.
Description du dispositif
Guidant EasyTrak 8 French Guiding Catheter, Inner Diameter .087'', 2.21 mm, Overall Length 44 cm, Coronary Sinus - Multi-Purpose Tip Shape, CS-MP, REF 6716
Manufacturer
Guidant Corp-Cpi Division
1 Event
Rappel de Device Recall Guidant
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Fabricant
Guidant Corp-Cpi Division
Adresse du fabricant
Guidant Corp-Cpi Division, 4100 Hamline Ave N, Saint Paul MN 55112-5700
Source
USFDA
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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
Manufacturer
Abbott Vascular-Cardiac Therapies dba Guidant Corporation
Device Recall Guidant VITALITY ICD
Modèle / numéro de série
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Worldwide
Description du dispositif
Guidant VITALITY VR/DR, Implantable Cardioverter Defibrillator, ICD, Models 1870 and 1871. Guidant VITALITY DR+, Implantable Cardioverter Defibrillator, ICD, Model 1872.
Manufacturer
Boston Scientific CRM Corp
Device Recall Guidant VITALITY AVT ICD
Modèle / numéro de série
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Worldwide
Description du dispositif
Guidant VITALITY AVT, Models A135 and A155. Implantable Cardioverter Defibrillator, ICD. Atrial and Ventricular Therapies. Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
Manufacturer
Boston Scientific CRM Corp
Device Recall Guidant ASSURE ICD
Modèle / numéro de série
Model B301: B301/100002, B301/100003, B301/100004, B301/100006, B301/100007, B301/100008, B301/100010, B301/100012, B301/100013, B301/100014, B301/100016, B301/100019, B301/100020, B301/100021, B301/100022, B301/100024, B301/100025, B301/100027, B301/100030, B301/100031, B301/100032, B301/100034, B301/100037, B301/100039, B301/100043, B301/100044, B301/100045, B301/100046, B301/100048, B301/100050, B301/100051, B301/100053, B301/100054, B301/100056, B301/100062, B301/100063, B301/100064, B301/100067, B301/100069, B301/100070, B301/100073, B301/100074, B301/100075, B301/100076, B301/100079, B301/100080, B301/100081, B301/100082, B301/100083, B301/100084, B301/100087, B301/100088, B301/100089, B301/100090, B301/100091, B301/100092, B301/100094, B301/100096, B301/100099, B301/100100, B301/100101, B301/100102, B301/100103, B301/100104, B301/100105, B301/100106, B301/100108, B301/100111, B301/100112, B301/100113, B301/100114, B301/100115, B301/100116, B301/100117, B301/100118, B301/100120, B301/100122, B301/100125, B301/100126, B301/100128, B301/100129, B301/100130, B301/100131, B301/100132, B301/100134, B301/100135, B301/100136, B301/100137, B301/100139, B301/100140, B301/100141, B301/100142, B301/100143, B301/100144, B301/100145, B301/100146, B301/100147, B301/100148, B301/100149, B301/100153, B301/100154, B301/100155, B301/100158, B301/100159, B301/100161, B301/100162, B301/100164, B301/100165, B301/100166, B301/100167, B301/100169, B301/100170, B301/100172, B301/100173, B301/100174, B301/100176, B301/100180, B301/100181, B301/100182, B301/100183, B301/100185, B301/100186, B301/100187, B301/100188, B301/100189, B301/100191, B301/100193, B301/100194, B301/100195, B301/100196, B301/100197, B301/100200, B301/100203, B301/100204, B301/100205, B301/100206, B301/100208, B301/100209, B301/100210, B301/100211, B301/100213, B301/100215, B301/100216, B301/100218, B301/100221, B301/100222, B301/100223, B301/100224, B301/100226, B301/100227, B301/100230, B301/100234, B301/100235, B301/100236, B301/100238, B301/100239, B301/100242, B301/100243, B301/100244, B301/100245, B301/100247, B301/100249, B301/100253, B301/100255, B301/100258, B301/100260, B301/100264, B301/100271, B301/100272, B301/100273, B301/100279, B301/100280, B301/100285, B301/100288, B301/100290, B301/100293, B301/100298, B301/100315, B301/100317, B301/100318
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Worldwide
Description du dispositif
Guidant ASSURE, Model B301, Implantable Cardioverter Defibrillator, ICD. (This model is not available in the USA) Guidant Corporation Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798, USA.
Manufacturer
Boston Scientific CRM Corp
Device Recall Guidant VITALITY ICD
Modèle / numéro de série
Classification du dispositif
Cardiovascular Devices
Classe de dispositif
3
Dispositif implanté ?
Yes
Distribution
Worldwide
Description du dispositif
Guidant VITALITY DS DR/VR (Models T125, T135), Guidant VITALITY EL (Model T127), Guidant VITALITY DR HE (Model T180), Implantable Cardioverter Defibrillators (ICD). Guidant Corporation, Cardiac Rhythm Management, 4100 Hamline Avenue North, St. Paul, MN 55112-5798 USA.
Manufacturer
Boston Scientific CRM Corp
40 en plus
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