FDA UDI In Commercial Distribution 🇺🇸 United States

TriMAX Implant System

DI: 00815432027583 · Model: TriMAX 25mm Prep Kit · CROSSROADS EXTREMITY SYSTEMS
Product Codes
1
GMDN Terms
5
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TriMAX Implant System
Primary DI
00815432027583
Version / Model
TriMAX 25mm Prep Kit
Catalog Number
7300-2500
Company Name
CROSSROADS EXTREMITY SYSTEMS
Labeler DUNS
058864308
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-17
Public Version
2
Public Version Date
2020-04-06
Public Version Status
Update
Public Device Record Key
136811db-df8d-4185-95c2-c87fd3fe5f06

Device Description

The TriMAX Implant System is a Nitinol Superelastic bone staple for use in surgery of the hand and foot for bone fragment osteotomy fixation and joint arthrodesis.

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
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
JDR Staple, Fixation, Bone

GMDN Terms

Code Name
47815 Orthopaedic implant aiming/guiding block, reusable
63198 Orthopaedic implant aiming/guiding block, single-use
36167 Orthopaedic broach
35095 Surgical drill guide, reusable
57789 Surgical drill guide, single-use

Identifiers

Type ID
Primary 00815432027583

Customer Contacts

Phone
901-221-8406