FDA UDI In Commercial Distribution 🇺🇸 United States

PROFIX

DI: 03596010225221 · Model: 71517114 · Smith & Nephew, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PROFIX
Primary DI
03596010225221
Version / Model
71517114
Catalog Number
71517114
Company Name
Smith & Nephew, Inc.
Labeler DUNS
045483575
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-30
Public Version
7
Public Version Date
2023-09-07
Public Version Status
Update
Public Device Record Key
4a2588d0-04b0-4eac-bd49-030506e6d61b

Device Description

PROFIX CONFORMING TIBIAL INSERT TRIAL RIGHT SIZE1 16MM

Device Characteristics

Single Use
No
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
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
58716 Knee tibia prosthesis trial, reusable

Identifiers

Type ID
Primary 03596010225221

Customer Contacts