MAHURKAR MANUFACTURED BY COVIDIEN LP, FORMERLY REGISTERED AS KENDALL

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Request for Information Form	Contact Information
Company Name	COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
Address	5439 STATE ROUTE 40
City, State, Zip	ARGYLE, NY 12809
Country	US
FDA Owner/Operator Phone	508-261-8587
FDA Medical Specialty Code	GU - Gastroenterology/Urology
FDA Product Code	NIE
FDA Classification Name	CATHETER, HEMODIALYSIS, TRIPLE LUMEN, NON-IMPLANTED
FDA Device Classification Code	Standards
FDA Regulation Number	876.5540
FDA Common Generic Name	TRIPLE LUMEN CATHETER, NON-IMPLANTED, MULTIPLE SIZES
FDA Proprietary Device Name	MAHURKAR
FDA Owner / Operator Number	1282497
FDA Owner / Operator Name	COVIDIEN LP, FORMERLY REGISTERED AS TYCO HEALTHCAR
FDA Establishment Registration Number	1317749
FDA Registered Establishment Name	COVIDIEN LP, FORMERLY REGISTERED AS KENDALL
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	06-10-02
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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1	LILY MEDICAL COMPANY 17595 HARVARD, C-182 IRVINE, CA 92614 US 949-280-0988 / 949-280-0988	VARIOUS MODELS HEMODIALYSIS BLOOD CATHETER	HEMODIALYSIS BLOOD CATHETER
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3	SU MEDICAL SUPPLIES 17595 HARVARD C-182 IRVINE, CA 92614 US 949-280-0988 / 949-280-0988	VARIOUS MODELS HEMODIALYSIS BLOOD CATHETER	HEMODIALYSIS BLOOD CATHETER