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
1479220776
Device Listing 1479220776
Listing Summary
#
Listing key
1479220776
Premarket submission
K112671
Device
STERILCONTAINER SYSTEM
Applicant
Aesculap, Ltd.
Product code
KCT
Decision date
2012-05-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
9103
9610612
3002806315
AESCULAP AG
1
N
2027-01-01
AM AESCULAP PLATZ TUTTLINGEN, DONAU Baden-Wurttemberg DE D-78532