FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653289066 · Model: JK091 · Aesculap AG
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
2

Basic Information

Brand Name
AESCULAP
Primary DI
04038653289066
Version / Model
JK091
Catalog Number
JK091
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
2
Record Status
Published
Publish Date
2016-09-23
Public Version
8
Public Version Date
2023-10-12
Public Version Status
Update
Public Device Record Key
0d9dfebd-6e1f-4a9d-a2ef-64950cf3fe0a

Device Description

Reusable Filter, package of 2 pieces, outer length: 95 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
Yes
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
KCT Sterilization wrap containers, trays, cassettes & other accessories
FLE Sterilizer, steam

GMDN Terms

Code Name
66887 Sterilization container filter, reusable

Identifiers

Type ID
Primary 04038653289066
Unit of Use 04038653346363

Customer Contacts