MENTOR COUDE 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	EZC
FDA Classification Name	CATHETER, COUDE
FDA Device Classification Code	Standards
FDA Regulation Number	876.5130
FDA Common Generic Name	COUDE CATHETER STERILE
FDA Proprietary Device Name	MENTOR COUDE 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)	MS - Specification Developer RR - Repackager/Relabeller
FDA Listing Date
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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