FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653394760 · Model: JM389 · Aesculap AG
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653394760
Version / Model
JM389
Catalog Number
JM389
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-23
Public Version
10
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
4a220095-3b41-4758-aa8f-3d39dd0b9062

Device Description

Inner Lid, Standard 1/2, outer length: 298 mm, outer width: 285 mm

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KCT Sterilization wrap containers, trays, cassettes & other accessories
FRG Wrap, sterilization

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04038653394760

Customer Contacts