FDA UDI In Commercial Distribution 🇺🇸 United States

ATTUNE

DI: 10603295543039 · Model: 1504-50-208 · DEPUY (IRELAND)
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
ATTUNE
Primary DI
10603295543039
Version / Model
1504-50-208
Catalog Number
150450208
Company Name
DEPUY (IRELAND)
Labeler DUNS
989365556
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-10-31
Public Version
1
Public Version Date
2025-11-10
Public Version Status
New
Public Device Record Key
76b0cdf7-edee-4ed6-8037-40331f918458

Device Description

ATTUNE KNEE SYSTEM REVISION HINGE FEMORAL 8 RIGHT CEMENTED CAUTION:INTENDED FOR CEMENTED USE ONLY

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
MR Conditional
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
KRO PROSTHESIS, KNEE, FEMOROTIBIAL, CONSTRAINED, CEMENTED, METAL/POLYMER

GMDN Terms

Code Name
33692 Rotating hinged total knee prosthesis

Identifiers

Type ID
Primary 10603295543039

Customer Contacts