Acerca de la base de datos
¿Cómo usar la IMDD?
Descargar la data
Preguntas frecuentes
Créditos
Devices
Device Recall KCI
Modelo / Serial
Serial numbers: IVAK00004, IVAK00023, IVAK00028, IVAK00034, IVAK00033, IVAK00032, IVAK00055, IVAK00060, IVAK00062, IVAK00063, IVAK00030, IVAK50000, IVAK00030, IVAK00035, IVAK00027, IVAK00054, IVAK00037, IVAK00041, IVAK00049, IVAK00044, IVAK00045, IVAK00046, IVAK00047, IVAK00048, IVAK00038, IVAK00039, IVAK00042, IVAK00043, IVAK00051, 000038251, 000038253, 000038295, 000038299
Clasificación del producto
Physical Medicine Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC
Descripción del producto
KCI Underbed Inverter, Accessory to Powered Flotation Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX. Model number 201189
Manufacturer
Kinetic Concepts, Inc
1 Event
Retiro De Equipo (Recall) de Device Recall KCI
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Fabricante
Kinetic Concepts, Inc
Dirección del fabricante
Kinetic Concepts, Inc, 4958 Stout Dr, San Antonio TX 78219-4334
Source
USFDA
3 dispositivos con un nombre similar
Más información acerca de la data
acá
Device Recall KCI TriaDyne Proventa
Modelo / Serial
The following serial numbers: TDBK00029, TDBK00294, TDBK00015, TDBK00291, TDBK00026, TDBK00027, TDBK00123, TDBK00124, TDBK00125, TDBK00127, TDBK00128, TDBK00130, TDBK00132, TDBK00136
Clasificación del producto
Physical Medicine Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC
Descripción del producto
KCI TriaDyne Proventa Critial Care Therapy System, manufactured by Kinetic Concepts, Inc., San Antonio, Texas 78219. Model number 308900
Manufacturer
Kinetic Concepts, Inc
Device Recall KCI Therapulse II
Modelo / Serial
Serial numbers: TPLK00053, TPLK00052, TPLK00011, TPLK00012, TPLK00013, TPLK00014, TPLK00015, TPLK00016, TPLK00124, TPLK00128, TPLK00132
Clasificación del producto
Physical Medicine Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Product was distributed domestically in the following states: IN, CA, NH, OR, PA, TX, WI, CO, IA, KS, MO, ID, MA, NC, IL, OH, MN, AZ, NE, HI, PR, NC
Descripción del producto
KCI Therapulse II Air Suspension Therapy Bed, manufactured by Kinetic Concepts, Inc., San Antonio, TX 78219. Model number 227080
Manufacturer
Kinetic Concepts, Inc
Device Recall KCI RotoProne Critical Care Therapy
Modelo / Serial
Serial numbers: RRFK0036-RRFK00047; RRFK00049-RRFK00115; RRFK00117-RRFK00128; RRFK00141-RRFK00211; RRFK00213-RRFK00233; RRFK00235; RRFK00237-RRRFK00254; RRFK00256-RRFK00261; RRFK00263-RRFK00267; RRFK00269-RRFK00270; RRFK00273-RRFK00280; RRFK00282-RRFK00284; RRFK00287-RRFK00290; and RRJK00002.
Clasificación del producto
Physical Medicine Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide Distribution - USA and Kuwait.
Descripción del producto
KCI RotoProne Critical Care Therapy System buckles for securing patient to the surface during proning therapy, Model 209500. || Indicated for treatment and prevention of pulmonary complications.
Manufacturer
KCI USA, Inc.
Language
English
Français
Español
한국어