FDA UDI In Commercial Distribution 🇺🇸 United States

DURALOC

DI: 10603295019671 · Model: 1245-80-058 · DEPUY (IRELAND)
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DURALOC
Primary DI
10603295019671
Version / Model
1245-80-058
Catalog Number
124580058
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2020-09-09
Public Version Status
Update
Public Device Record Key
948f7864-059c-4528-ade8-384c4a84d3ce

Device Description

DURALOC SHELL SECTOR 66mm OD CEMENTLESS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JDI Prosthesis, hip, semi-constrained, metal/polymer, cemented
LPH PROSTHESIS, HIP, SEMI-CONSTRAINED, METAL/POLYMER, POROUS UNCEMENTED

GMDN Terms

Code Name
43167 Acetabular shell

Identifiers

Type ID
Primary 10603295019671

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K951301 000
K952740 000
K961186 000