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Preguntas frecuentes
Créditos
Devices
ProVision Barrier Universal Hood/Gown; product 5431-33-000
Modelo / Serial
All product manufactured between February 1, 2002 and June 17, 2003 that does not have a green square on the label above the CE mark. Product bearing the green square on the label has been 100% inspected and is not under recall.
Clasificación del producto
General Hospital and Personal Use Devices
Clase de dispositivo
2
¿Implante?
No
Distribución
United States, Australia, Canada, Chile, England, India, Japan, Malaysia, Singapore, South Africa, Taiwan and United Kingdom
Descripción del producto
ProVision Barrier Universal Hood/Gown; product 5431-33-000
Manufacturer
Depuy Orthopaedics, Inc.
1 Event
Retiro De Equipo (Recall) de ProVision Barrier Universal Hood/Gown; product 5431-33-000
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Fabricante
Depuy Orthopaedics, Inc.
Dirección del fabricante
Depuy Orthopaedics, Inc., 700 Orthopaedic Drive, Warsaw IN 46581
Source
USFDA
Language
English
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