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Crédits
Devices
Device Recall Access SystemGI Monitor
Modèle / numéro de série
all lots
Classification du dispositif
Immunology and Microbiology Devices
Classe de dispositif
2
Dispositif implanté ?
No
Distribution
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
Description du dispositif
Access System-GI Monitor (CA19-9), A83873D, Catalog No. 387687
Manufacturer
Beckman Coulter Inc.
1 Event
Rappel de Device Recall Access SystemGI Monitor
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Fabricant
Beckman Coulter Inc.
Adresse du fabricant
Beckman Coulter Inc., 250 S Kraemer Blvd, Brea CA 92821-6232
Société-mère du fabricant (2017)
Danaher Corporation
Source
USFDA
Language
English
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