FDA UDI In Commercial Distribution 🇺🇸 United States

Timberline Lateral Fusion System

DI: 03662663274128 · Model: 8734-6120 · 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
03662663274128
Version / Model
8734-6120
Catalog Number
8734-6120
Company Name
Highridge Medical, LLC
Labeler DUNS
119260394
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-18
Public Version
1
Public Version Date
2025-12-26
Public Version Status
New
Public Device Record Key
e1aa06c3-c950-40d6-b1d4-ce93fd86a880

Device Description

SCREW EXTRACTOR

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
HWB EXTRACTOR

GMDN Terms

Code Name
12696 Orthopaedic inorganic implant inserter/extractor, reusable

Identifiers

Type ID
Primary 03662663274128

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Device Size Text, specify---SCREW EXTRACTOR