À propos de cette base de données
Comment utiliser cette base de données
Téléchargez les données
FAQ
Crédits
Devices
Device Recall AutoMate 2500 Family
Modèle / numéro de série
All systems up to the following Serial Numbers: ODL25120 Revision T; SN3101, ODL25125 Revision W; SN1508, ODL25250 Revision T; SN2416, ODL25255 Revision W; SN4617
Classification du dispositif
Clinical Chemistry and Clinical Toxicology Devices
Classe de dispositif
1
Dispositif implanté ?
No
Distribution
Australia, Austria, Belarus, Belgium, Bosnia and Herzegovina, Brazil, Canada, China, Croatia, Cyprus, Czech Republic, Denmark, Finland, France, Germany, Gibraltar, Greece, Hong Kong, Hungary, India, Ireland, Israel, Italy, Korea, Kuwait, Latvia, Lithuania, Macao, Mayotte, Mexico, Netherlands, New Zealand, Norway, Panama, Poland, Portugal, Qatar, Russia, Saudi Arabia, Singapore, Slovakia, Slovenia, South Africa, Spain, Sweden, Switzerland, Taiwan, Turkey, United Kingdom, United States
Description du dispositif
AutoMate 1200 Catalog Number ODL25120; || AutoMate 1250 Catalog Number ODL25125; || AutoMate 2500 Catalog Number ODL25250; || AutoMate 2550 Catalog Number ODL25255
Manufacturer
Beckman Coulter Inc.
1 Event
Rappel de Device Recall AutoMate 2500 Family
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
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
Français
Español
한국어