FDA UDI In Commercial Distribution 🇺🇸 United States

SIGMA RPF AOX

DI: 10603295075752 · Model: 1961-91-013 · DEPUY ORTHOPAEDICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SIGMA RPF AOX
Primary DI
10603295075752
Version / Model
1961-91-013
Catalog Number
196191013
Company Name
DEPUY ORTHOPAEDICS, INC.
Labeler DUNS
080506581
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-03-24
Public Version
5
Public Version Date
2021-10-11
Public Version Status
Update
Public Device Record Key
ecf8a75a-60eb-42f6-9bc1-8f55d33ad970

Device Description

SIGMA TIBIAL INSERT ROTATING PLATFORM RPF AOX SIZE 1 17.5mm

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
NJL Prosthesis, knee, patellofemorotibial, semi-constrained, metal/polymer, mobile bearing

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary 10603295075752

Customer Contacts