VIAMED RECTAL ILEOSTOMY CATHETER MANUFACTURED BY RECE INTERNATIONAL CORP.

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Request for Information Form	Contact Information
Company Name	RECE INTERNATIONAL CORP.
Address	5881 N.W. 151ST ST., STE. 111
City, State, Zip	MIAMI LAKES, FL 33014
Country	US
FDA Owner/Operator Phone	305-362-6555
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	CONTINENT ILEOSTOMY CATHETER
FDA Proprietary Device Name	VIAMED RECTAL ILEOSTOMY CATHETER
FDA Owner / Operator Number	9071876
FDA Owner / Operator Name	RECE INTERNATIONAL CORP.
FDA Establishment Registration Number	3003965134
FDA Registered Establishment Name	RECE INTERNATIONAL CORP.
FDA Operation Code(s)	RR - Repackager/Relabeller
FDA Listing Date	01-19-06
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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