FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04038653294923 · Model: JN440 · Aesculap AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04038653294923
Version / Model
JN440
Catalog Number
JN440
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
b16b0aee-1ea8-4f08-a745-e9554494aa8b

Device Description

Bottom, with base perforation, Standard 1/1, outer length: 592 mm, outer width: 274 mm, outer heigth: 90 mm, inner length: 544 mm, inner width: 258 mm, inner heigth: 75 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
FLE Sterilizer, steam
KCT Sterilization wrap containers, trays, cassettes & other accessories

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04038653294923

Customer Contacts