GEUDER MICRO-KERATRON TREPHINE SYSTEM MANUFACTURED BY GEUDER AG

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Request for Information Form	Contact Information
Company Name	GEUDER AG
Address	HERTZSTRASSE 4
City, State, Zip	HEIDELBERG,
Country	GM
FDA Owner/Operator Phone	490-62-213066
FDA Medical Specialty Code	OP - Opthalmic
FDA Product Code	HRG
FDA Classification Name	ENGINE, TREPHINE, ACCESSORIES, AC-POWERED
FDA Device Classification Code	General Controls
FDA Regulation Number	886.4070
FDA Common Generic Name	GEUDER MICRO-KERATRON TREPHINE SYSTEM
FDA Proprietary Device Name	GEUDER MICRO-KERATRON TREPHINE SYSTEM
FDA Owner / Operator Number	9024476
FDA Owner / Operator Name	GEUDER AG
FDA Establishment Registration Number	9616245
FDA Registered Establishment Name	GEUDER AG
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	08-30-96
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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