FDA UDI In Commercial Distribution 🇺🇸 United States

Timberline Lateral Fusion System

DI: 03662663266406 · Model: 8732-5117 · Highridge Medical, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Timberline Lateral Fusion System
Primary DI
03662663266406
Version / Model
8732-5117
Catalog Number
8732-5117
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-16
Public Version
1
Public Version Date
2025-11-24
Public Version Status
New
Public Device Record Key
6c1ca18d-9a06-4e24-b5df-285c2a271d04

Device Description

PADDLE SHAVER 17MM

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
No
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
35090 Surgical gouge

Identifiers

Type ID
Primary 03662663266406

Customer Contacts