CORTICOSTERONE TEST SYSTEM MANUFACTURED BY DRG INSTRUMENTS GMBH

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Request for Information Form	Contact Information
Company Name	DRG INSTRUMENTS GMBH
Address	FRAUENBERGSTRASSE 18
City, State, Zip	MARBURG,
Country	GM
FDA Owner/Operator Phone	908-233-2079
FDA Medical Specialty Code	CH - Clinical Chemistry
FDA Product Code	CHA
FDA Classification Name	RADIOIMMUNOASSAY, CORTICOSTERONE
FDA Device Classification Code	General Controls
FDA Regulation Number	862.1200
FDA Common Generic Name	CORTICOSTERONE
FDA Proprietary Device Name	CORTICOSTERONE TEST SYSTEM
FDA Owner / Operator Number	2245285
FDA Owner / Operator Name	DRG INTL., INC.
FDA Establishment Registration Number	3002800697
FDA Registered Establishment Name	DRG INSTRUMENTS GMBH
FDA Operation Code(s)	MM - Manufacturer MR - Remanufacturer RR - Repackager/Relabeller
FDA Listing Date	09-09-05
FDA Listing Status Code	Active
Differentiation	N/A
Keywords	N/A
Description	N/A
Brochure	N/A
Product Website	N/A

Our records indicate that the following medical device companies may manufacture a similar device.

	Company Name / Address / Phone	Proprietary Device Name	Common Generic Device Name
1	AMERICAN LABORATORY PRODUCTS CO., LTD. 26 KEEWAYDIN DR., UNIT G SALEM, NH 03079 US 603-893-8914 / 603-893-8914	ALPCO DIAGNOSTICS CORTICOSTERONE ELISA	CORTICOSTERONE ELISA
2	DEMEDITEC DIAGNOSTICS LISE-MEITNER-STRASSE 2 KIEL-WELLSEE, D-24145 GM 49-431-7192251 / 763-780-2955	IBL AMERICA CORTICOSTERONE ELISA TEST KIT	CORTICOSTERONE ELISA TEST KIT