FDA UDI In Commercial Distribution 🇺🇸 United States

ATTUNE

DI: 10603295477808 · Model: 2512-14-050 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATTUNE
Primary DI
10603295477808
Version / Model
2512-14-050
Catalog Number
251214050
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-12-05
Public Version
4
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
88c8993a-7005-4694-89b4-b8abb9a477f5

Device Description

ATTUNE KNEE SYSTEM REVISION CEMENTED STEM TRIAL 14mm X 50mm

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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10603295477808

Customer Contacts