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
1079568442
Device Listing 1079568442
Listing Summary
#
Listing key
1079568442
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
22908
1000649241
1000649241
Bort GmbH
1
N
2026-01-01
Am Schweizerbach 1 WEINSTADT-BENZACH Baden-Wurttemberg DE 71384