ANTI-HUMAN FIBRINOGEN, FITC MANUFACTURED BY DIASORIN, INC.

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Request for Information Form	Contact Information
Company Name	DIASORIN, INC.
Address	1951 NORTHWESTERN AVE. P.O. BOX 285
City, State, Zip	STILLWATER, MN 55082
Country	US
FDA Owner/Operator Phone	390-161-487 093
FDA Medical Specialty Code	HE - Hematology
FDA Product Code	DAX
FDA Classification Name	FIBRINOGEN AND SPLIT PRODUCTS, FITC, ANTIGEN, ANTISERUM, CONTROL
FDA Device Classification Code	Standards
FDA Regulation Number	864.7340
FDA Common Generic Name	ANTI-HUMAN FIBRINOGEN, FLUORESCEIN CONJUGATE
FDA Proprietary Device Name	ANTI-HUMAN FIBRINOGEN, FITC
FDA Owner / Operator Number	9051149
FDA Owner / Operator Name	DIASORIN S.P.A.
FDA Establishment Registration Number	2182595
FDA Registered Establishment Name	DIASORIN, INC.
FDA Operation Code(s)
FDA Listing Date	04-28-95
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. 1000 LAKE HAZELTINE DR. CHASKA, MN 55318 US 714-871-4848 / 714-993-5321 8383	FIBRINOGEN FLUORESCEIN CONJUGATED ANTISERA	FIBRINOGEN FLUORESCEIN CONJUGATED ANTISERA
2	KENT LABORATORIES, INC. 777 JORGENSEN PLACE BELLINGHAM, WA 98226 US 360-398-8641 / 360-398-8641	FITC CONJUGATED ANTI HUMAN FIBRINOGEN