FDA UDI In Commercial Distribution 🇺🇸 United States

Timberline Lateral Fusion System

DI: 03662663276214 · Model: 8737-7257 · 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
03662663276214
Version / Model
8737-7257
Catalog Number
8737-7257
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
415c12d0-5729-48b0-8efa-33609d8af136

Device Description

RONGEUR PITUITARY ANG RT BLK CERAMIC 7MM

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
HTX RONGEUR

GMDN Terms

Code Name
35541 Spinal rongeur

Identifiers

Type ID
Primary 03662663276214

Customer Contacts