gudid
Primary ID: 69-RG-2015
Dakota ALIF System (UDI 69-RG-2015)
Manufactured by PRECISION SPINE, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Dakota ALIF System - Primary ID 69-RG-2015
Device Regulatory Overview
The Dakota ALIF System (Model/Catalog Number: 69-RG-2015) is a medical device manufactured by PRECISION SPINE, INC.. This product is indexed under FDA Product Code / Category Classification HTR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 69-RG-2015
- Product Code / EMDN
- HTR
- Device Name
- 39 X 29 X 15mm X 20 Trial Rasp
- Database Sync Date
- 2026-08-09 09:33:11
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Dakota ALIF System?
The registered manufacturer of record for Dakota ALIF System is PRECISION SPINE, INC..
What is the Primary UDI-DI identifier for Dakota ALIF System?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 69-RG-2015.
What classification code is assigned to this device?
This device is registered under product classification code HTR.
Similar Classification Devices (HTR)
Other Devices by PRECISION SPINE, INC.
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