HEMAPROMPT MANUFACTURED BY AERSCHER DIAGNOSTICS

Please Login or Create an Account Now.

This company has been viewed 18 times within the past 60 days.

This product has been viewed: 2 times.

Request for Information Form	Contact Information
Company Name	AERSCHER DIAGNOSTICS
Address	353 HIGH ST.
City, State, Zip	CHESTERTOWN, MD 21620
Country	US
FDA Owner/Operator Phone	410-778-1144
FDA Medical Specialty Code	HE - Hematology
FDA Product Code	GGG
FDA Classification Name	GUAIAC REAGENT
FDA Device Classification Code	Standards
FDA Regulation Number	864.6550
FDA Common Generic Name	HEMAPROMPT-FECAL OCCULT BLOOD KIT, HEMASCREEN SEAT COLONCHECK
FDA Proprietary Device Name	HEMAPROMPT
FDA Owner / Operator Number	9007799
FDA Owner / Operator Name	AERSCHER DIAGNOSTICS
FDA Establishment Registration Number	1123776
FDA Registered Establishment Name	AERSCHER DIAGNOSTICS
FDA Operation Code(s)	MM - Manufacturer
FDA Listing Date	09-01-93
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	BECKMAN COULTER, INC. 606 ELMWOOD AVE. SHARON HILL, PA 19079 US 714-871-4848 / 714-993-5321 8383	HEMOCULT, HEMOCCULTSENSA	FECAL OCCULT BLOOD TEST
2	EMD CHEMICALS INC. 480 DEMOCRAT RD. GIBBSTOWN, NJ 08027 US 011-49-6151726060 / 856-423-6300 315	NO PROPRIETARY NAME LISTED	NO COMMON NAME LISTED