Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1993898598
Device Listing 1993898598
Listing Summary
#
Listing key
1993898598
Premarket submission
K053012
Device
FIDIS VASCULITIS, MODEL MX007
Applicant
Biomedical Diagnostics (Bmd) SA
Product code
MOB
Decision date
2006-03-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
63825
3003935253
3003935253
THERADIAG
1
N
2026-01-01
14 rue AMBROISE CROIZAT CS 90136 CROISSY BEAUBOURG MARNE LA VALLEE CEDEX 2 Seine-et-Marne FR 77435