FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653131068 · Model: JK817 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653131068
Version / Model
JK817
Catalog Number
JK817
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-05-19
Public Version
7
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
8e26b25d-bc22-404f-8ab4-b78a5cb6723a

Device Description

Bottom, without base perforation, outer length: 589 mm, outer width: 363 mm, outer heigth: 107 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
FRG Wrap, sterilization

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04038653131068

Customer Contacts