FDA UDI In Commercial Distribution 🇺🇸 United States

Timberline Lateral Fusion System

DI: 03662663275071 · Model: 8737-5105 · 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
03662663275071
Version / Model
8737-5105
Catalog Number
8737-5105
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
a312c9ff-9196-4997-bce0-6c826bb3938b

Device Description

CURETTE 15D ANG UP STRT THIN SHAFT SZ 5

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
HTF CURETTE

GMDN Terms

Code Name
31335 Bone curette, reusable

Identifiers

Type ID
Primary 03662663275071

Customer Contacts