ASTRA TECH AB MANUFACTURED BY ASTRA TECH AB

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Request for Information Form	Contact Information
Company Name	ASTRA TECH AB
Address	AMINOGATAN 1
City, State, Zip	MOLNDAL,
Country	SW
FDA Owner/Operator Phone	44-207-304 5000
FDA Medical Specialty Code	GU - Gastroenterology/Urology
FDA Product Code	KPH
FDA Classification Name	CATHETER, RECTAL FOR CONTINENT ILEOSTOMY
FDA Device Classification Code	General Controls
FDA Regulation Number	876.5030
FDA Common Generic Name	ILEOSTOMY CATHETER
FDA Proprietary Device Name	ASTRA TECH AB
FDA Owner / Operator Number	8032019
FDA Owner / Operator Name	ASTRAZENECA PLC
FDA Establishment Registration Number	9612468
FDA Registered Establishment Name	ASTRA TECH AB
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	06-18-98
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

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