FDA UDI In Commercial Distribution 🇺🇸 United States

TM Ardis Interbody System

DI: 03662663067713 · Model: 06-701-05141 · Highridge Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TM Ardis Interbody System
Primary DI
03662663067713
Version / Model
06-701-05141
Catalog Number
06-701-05141
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-13
Public Version
1
Public Version Date
2025-11-21
Public Version Status
New
Public Device Record Key
08b74bad-4b93-43bd-ab79-8c9f818bb104

Device Description

TM Ardis® Interbody System

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
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 03662663067713

Customer Contacts