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Preguntas frecuentes
Créditos
Devices
Device Recall Access SystemGI Monitor
Modelo / Serial
all lots
Clasificación del producto
Immunology and Microbiology Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
Algeria, Angola, Australia, Austria, Bangladesh, Belgium, Bolivia, Bosnia and Herzegovina, Botswana, Brazil, Brunei, Bulgaria, Canada, Chile, China, Colombia, Costa Rica, Croatia, Cyprus, Czech Republic, Denmark, Djibouti, Ecuador, Egypt, El Salvador, Estonia, Ethiopia, Finland, France, Georgia, Germany, Ghana, Gibraltar, Greece, Guam, Guatemala, Honduras, Hong Kong, Hungary, India, Indonesia, Ireland, Israel, Italy, Japan, Jordan, Kazakhstan, Kenya, Kuwait, Lebanon, Libya, Lithuania, Macau, Malawi, Malaysia, Mayotte, Mexico, Morocco, Myanmar, Namibia, Nepal, Netherlands, Netherlands Antillean, New Zealand, Nigeria, Norway, Oman, Pakistan, Panama, Paraguay, Peru, Philippines, Poland, Portugal, Puerto Rico, Qatar, Romania, Russia, Rwanda, Saudi Arabia, Serbia, Sierra Leone, Singapore, Slovakia, South Africa, South Korea, Spain, Sri Lanka, Swaziland, Sweden, Switzerland, Taiwan, Thailand, Tunisia, Turkey, Uganda, United Arab Emirates, United Kingdom, United States, Uruguay, Venezuela, Vietnam, Zambia, Zimbabwe
Descripción del producto
Access System-GI Monitor (CA19-9), A83873D, Catalog No. 387687
Manufacturer
Beckman Coulter Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall Access SystemGI Monitor
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Fabricante
Beckman Coulter Inc.
Dirección del fabricante
Beckman Coulter Inc., 250 S Kraemer Blvd, Brea CA 92821-6232
Empresa matriz del fabricante (2017)
Danaher Corporation
Source
USFDA
Language
English
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