FDA UDI Not in Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964055645 · Model: XG397 · Aesculap AG
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964055645
Version / Model
XG397
Catalog Number
XG397
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-10
Public Version
12
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
50bc1441-589a-4cd8-9e5b-b2961eac582f
Distribution End Date
2020-05-31

Device Description

Bottom, without base perforation, Standard 1/1, outer length: 592 mm, outer width: 274 mm, outer heigth: 120 mm, inner length: 544 mm, inner width: 258 mm, inner heigth: 105 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
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

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 04046964055645

Customer Contacts