FDA UDI In Commercial Distribution 🇺🇸 United States

ATTUNE

DI: 10603295513681 · Model: 2999-66-504 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ATTUNE
Primary DI
10603295513681
Version / Model
2999-66-504
Catalog Number
299966504
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-08-12
Public Version
2
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
065bc857-956a-4f05-a719-e28231ee8500

Device Description

ATTUNE MAKE TO ORDER 2 DEGREE POSTERIOR TIBIAL SYMMETRICAL RE-CUT BLOCK

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
HTZ INSTRUMENT, CUTTING, ORTHOPEDIC

GMDN Terms

Code Name
13180 Orthopaedic prosthesis implantation positioning instrument, reusable

Identifiers

Type ID
Primary 10603295513681

Customer Contacts