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
1356728202
Device Listing 1356728202
Listing Summary
#
Listing key
1356728202
Premarket submission
K243720
Device
3Delta UNlimited
Applicant
Deltamed GmbH
Product code
EBF
Decision date
2024-12-18
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
138552
3009432160
3009432160
anax USA
1
Y
2026-01-01
406 I ST NW ARDMORE Ardmore OK US 73401