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
1368142275
Device Listing 1368142275
Listing Summary
#
Listing key
1368142275
Premarket submission
P130027
Device
ARTUS CMV RGQ MDX KIT
Applicant
QIAGEN, INC.
Product code
PAB
Decision date
2014-06-02
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
23249
3004013603
3004013603
QIAGEN, GMBH
1
N
2026-01-01
QIAGEN STRASSE 1 HILDEN North Rhine-Westphalia DE 40724