FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653228133 · Model: JK089 · Aesculap AG
Product Codes
3
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

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Basic Information

Brand Name
AESCULAP
Primary DI
04038653228133
Version / Model
JK089
Catalog Number
JK089
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2016-09-23
Public Version
10
Public Version Date
2025-07-03
Public Version Status
Update
Public Device Record Key
45abd62b-ac10-4aaf-8c12-b69b8b4674fa

Device Description

Paper Filter, package of 10 pieces, outer length: 225 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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

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

GMDN Terms

Code Name
66887 Sterilization container filter, reusable

Identifiers

Type ID
Primary 04038653228133
Unit of Use 04038653342754

Customer Contacts