Aniara Diagnostica L L C

FDA Filings

This page includes the latest FDA filings for Aniara Diagnostica L L C. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Aniara Diagnostica L L C holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3005017664
FEI Number3005017664
NameANIARA DIAGNOSTICA, LLC
Owner & OperatorANIARA DIAGNOSTICA, LLC
Contact Address7768 Service Center Drive
West Chester OH 45069 US
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address7768 Service Center Dr
West Chester, OH 45069 US

FDA Filings

Device
Company
DeviceDate
ANIARA DIAGNOSTICA ,LLC
HEMOCLOT QUANTI- V-L, FACTOR V-L CALIBRATOR, BIOPHEN V-L CAL (UNDILUTED), BIOPHEN ACT. PC-R CONTROL PLASMA AND BIOPHEN2009-05-08

Related Finance Registrations
NCAGE Code5MWV2ANIARA DIAGNOSTICA LLC
CAGE Code5MWV2ANIARA DIAGNOSTICA LLC
DUNS830505058Aniara Diagnostica LLC
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.