FDA UDI In Commercial Distribution 🇺🇸 United States

Triathlon

DI: 07613327015461 · Model: 5542-A-802 · Howmedica Osteonics Corp.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Triathlon
Primary DI
07613327015461
Version / Model
5542-A-802
Catalog Number
5542-A-802
Company Name
Howmedica Osteonics Corp.
Labeler DUNS
058311945
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-24
Public Version
4
Public Version Date
2023-02-03
Public Version Status
Update
Public Device Record Key
6239efcd-41c7-48c8-a692-9d03b8e009c8

Device Description

Femoral Distal Augment

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MBH PROSTHESIS, KNEE, PATELLO/FEMOROTIBIAL, SEMI-CONSTRAINED, UNCEMENTED, POROUS, COATED, POLYMER/METAL/POLYMER
JWH PROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

GMDN Terms

Code Name
48067 Knee arthroplasty wedge

Identifiers

Type ID
Primary 07613327015461

Device Sizes

Type Value Unit Text
Device Size Text, specify Side: RIGHT
Device Size Text, specify Size: 8
Device Size Text, specify Thickness: 15.0 Millimeter