Acerca de la base de datos
¿Cómo usar la IMDD?
Descargar la data
Preguntas frecuentes
Créditos
Devices
Device Recall Conserve Shells
Modelo / Serial
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
2
¿Implante?
Yes
Distribución
Worldwide Distribution - US (nationwide) Argentina, Australia, Austria, Belgium, Brazil, Bulgaria, Canada, China, Columbia, Cyprus, Czech Republic, Denmark, Finland, France, Georgia, Germany, Greece, Iran, Italy, Jamaica, Japan, Lithuania, Malaysia, Philippines, Poland, Portugal, Russia, Slovenia, South Africa, South Korea, Spain, Switzerland, Taiwan, Netherlands, Turkey, Arab Emirates, United Kingdom, and Vietnam.
Descripción del producto
Conserve Shells: REF 38021146, REF 38021148, REF 38021150, REF 38021152, REF 38021154, REF 38021156, REF 38021158, REF 38021160, REF 38021162, REF 38021164, REF 38023642, REF 38023646, REF 38023844, REF 38023848, REF 38024046, REF 38024050, REF 38024248, REF 38024252, REF 38024450, REF 38024454, REF 38024652, REF 38024656, REF 38024854, REF 38024858, REF 38025056, REF 38025060, REF 38025258, REF 38025262, REF 38025460, REF 38025464, REF 38025662, REF 38025664, REF 38025666, REF 38025668, REF 38123844, REF 38124046, REF 38124248, REF 38124450, REF 38125056, REF 38125662, REF 38HA3642, REF 38HA3844, REF 38HA4046, REF 38HA4248, REF 38HA4450, REF 38HA4652, REF 38HA4854, REF 38HA5056, REF 38HA5258, REF 38HA5460, REF 38HA5662, REF 38HA5664, REF 38HA5864, REF 38HA6066, REF 38SP3642, REF 38SP3844, REF 38SP4046, REF 38SP4248, REF 38SP4450, REF 38SP4652, REF 38SP4854, REF 38SP5056, REF 38SP5258, REF 38SP5460, REF 38SP5662, REF 38SP5664 || For use with the conserve metal head
Manufacturer
MicroPort Orthopedics Inc.
1 Event
Retiro De Equipo (Recall) de Device Recall Conserve Shells
{{ $t('card.reduce') }}
{{ $tc('card.more', left) }}
Fabricante
MicroPort Orthopedics Inc.
Dirección del fabricante
MicroPort Orthopedics Inc., 5677 Airline Rd, Arlington TN 38002-9501
Empresa matriz del fabricante (2017)
Shanghai Microport Medical (Group) Co. Ltd.
Source
USFDA
Language
English
Français
Español
한국어