FDA UDI In Commercial Distribution 🇺🇸 United States

DURALOC

DI: 10603295108337 · Model: 2252-44-503 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DURALOC
Primary DI
10603295108337
Version / Model
2252-44-503
Catalog Number
225244503
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
2
Public Version Date
2019-02-07
Public Version Status
Update
Public Device Record Key
aebd2b18-0add-4970-bd15-19e248f4e0fc

Device Description

DURALOC BANTAM TRIAL SIZER 44mmOD

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
58481 Femoral stem prosthesis trial

Identifiers

Type ID
Primary 10603295108337

Customer Contacts