NO PROPRIETARY NAME LISTED MANUFACTURED BY DRG INTL., INC.

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Request for Information Form	Contact Information
Company Name	DRG INTL., INC.
Address	1167 US HIGHWAY 22
City, State, Zip	MOUNTAINSIDE, NJ 07092
Country	US
FDA Owner/Operator Phone	908-233-2079
FDA Medical Specialty Code	OB - Obstetrics/Gynecology
FDA Product Code	HEI
FDA Classification Name	MONITOR, HEART-VALVE MOVEMENT, FETAL, ULTRASONIC
FDA Device Classification Code	Standards
FDA Regulation Number	884.2660
FDA Common Generic Name	NO COMMON NAME LISTED
FDA Proprietary Device Name	NO PROPRIETARY NAME LISTED
FDA Owner / Operator Number	2245285
FDA Owner / Operator Name	DRG INTL., INC.
FDA Establishment Registration Number	2245285
FDA Registered Establishment Name	DRG INTL., INC.
FDA Operation Code(s)
FDA Listing Date
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	CONTRACT MEDICAL MANUFACTURING LLC 1 JACKS HILL ROAD OXFORD, CT 06478 US 203-888-1430 / 203-888-1430 33	DRG REACTION CHAMBER/SAFETY TIP	ULTRASONIC HEART VALVE MONITOR
2	MEDGYN PRODUCTS, INC. 328 NORTH EISENHOWER LN. LOMBARD, IL 60148 US 630-627-4105 / 630-627-4105		DETECTOR, FETAL HEART, ULTRASONIC (DOPPLER)