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Créditos
Devices
Device Recall Disetronic
Modelo / Serial
Lot 3H003UF.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Descripción del producto
Disetronic Ultraflex 8/60 infusion set; (Distributed outside of the US only).
Manufacturer
Disetronic Medical Systems, Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall Disetronic
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Fabricante
Disetronic Medical Systems, Inc.
Dirección del fabricante
Disetronic Medical Systems, Inc., 11800 Exit 5 Parkway, Suite 120, Fishers IN 46038
Source
USFDA
4 dispositivos con un nombre similar
Más información acerca de la data
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Device Recall Disetronic DTron
Modelo / Serial
All units with the following lot numbers being used by patients 13 years of age or younger: lots 4013674 through 4022628. The last affected lot expires in April 2007.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Nationwide.
Descripción del producto
Disetronic D-Tronplus Insulin Pump adapters; Ref 3000803; catalog reference number 0457243001 sold in packages of ten adapters.
Manufacturer
Roche Diagnostics Corp.
Device Recall Disetronic
Modelo / Serial
Lot 3G039UF.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Descripción del producto
Disetronic Ultraflex 8/80 infusion set; Catalog number 4489039001. (Distributed outside of the US only).
Manufacturer
Disetronic Medical Systems, Inc.
Device Recall Disetronic
Modelo / Serial
Lot 3J012UF.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Descripción del producto
Disetronic Ultraflex 8/110 infusion set; (Distributed outside of the US only).
Manufacturer
Disetronic Medical Systems, Inc.
Device Recall Disetronic
Modelo / Serial
Lot 3H067UF.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Worldwide including USA, Argentina, Austria, Barbados, Belgium, Canada, Czech Republic, Denmark, Estonia, Finland, France, Germany, Greece, Honduras, Hungary, Italy, Mexico, Netherlands, New Zealand, Norway, Poland, Portugal, Singapore, Slovenia, Spain, Sweden, Switzerland and United Kingdom.
Descripción del producto
Disetronic Ultraflex 10/110 infusion set; (Distributed outside of the US only).
Manufacturer
Disetronic Medical Systems, Inc.
Language
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