FDA UDI In Commercial Distribution 🇺🇸 United States

Timberline Lateral Fusion System

DI: 03662663269209 · Model: 8733-3108 · 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
03662663269209
Version / Model
8733-3108
Catalog Number
8733-3108
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-11-17
Public Version
1
Public Version Date
2025-11-25
Public Version Status
New
Public Device Record Key
446d0c64-d8f9-4788-b817-9d664d07f572

Device Description

SCRAPER O'BRIEN 8MM

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
31335 Bone curette, reusable

Identifiers

Type ID
Primary 03662663269209

Customer Contacts