FDA UDI In Commercial Distribution 🇺🇸 United States

AESCULAP

DI: 04046964962103 · Model: MD151 · Aesculap AG
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AESCULAP
Primary DI
04046964962103
Version / Model
MD151
Catalog Number
MD151
Company Name
Aesculap AG
Labeler DUNS
315018218
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-12-07
Public Version
4
Public Version Date
2023-04-04
Public Version Status
Update
Public Device Record Key
9ed79a19-943a-46e3-bdaf-649edeee61c3

Device Description

Lid (Outer), with label hanger, aluminium anodized, silver, outer length: 319 mm, outer width: 190 mm, outer heigth: 25 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
FLE Sterilizer, steam

GMDN Terms

Code Name
13730 Device sterilization/disinfection container, reusable

Identifiers

Type ID
Primary 04046964962103

Customer Contacts