CONTINENT ILEO SILICONE CATHETER MANUFACTURED BY COLOPLAST MANUFACTURING US, LLC

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Request for Information Form	Contact Information
Company Name	COLOPLAST MANUFACTURING US, LLC
Address	1615 WEST RIVER RD., NORTH
City, State, Zip	MINNEAPOLIS, MN 55411
Country	US
FDA Owner/Operator Phone	45-49-111111
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	STERILE RECTAL CATHETER FOR CONTINENT ILEOSTOMY
FDA Proprietary Device Name	CONTINENT ILEO SILICONE CATHETER
FDA Owner / Operator Number	8010144
FDA Owner / Operator Name	COLOPLAST A/S
FDA Establishment Registration Number	2183558
FDA Registered Establishment Name	COLOPLAST MANUFACTURING US, LLC
FDA Operation Code(s)	MM - Manufacturer MS - Specification Developer
FDA Listing Date	12-29-93
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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5	REACH GLOBAL INDUSTRIES, INC. 8 CORPORATE PARK, SUITE 300 IRVINE, CA 92606 US 888-518-8389 / 949-486-1881	MULTIPLE	STERILE RECTAL CATHETER FOR CONTINENT ILEOSTOMY
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