FDA UDI In Commercial Distribution 🇺🇸 United States

DURALOC

DI: 10603295108146 · Model: 2248-10-000 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DURALOC
Primary DI
10603295108146
Version / Model
2248-10-000
Catalog Number
224810000
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-24
Public Version
3
Public Version Date
2020-12-21
Public Version Status
Update
Public Device Record Key
4dbf6ef4-9b63-4466-9be7-7d7c7c79c8ea

Device Description

DURALOC TRIAL LINER 28mm ID 50mm OD +4

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
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
Yes
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
HWT TEMPLATE

GMDN Terms

Code Name
58480 Acetabulum prosthesis trial, prefabricated, reusable

Identifiers

Type ID
Primary 10603295108146

Customer Contacts