gudid
Primary ID: KS0L-M
Prodia Select (UDI KS0L-M)
Manufactured by ABRASIVE TECHNOLOGY, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Prodia Select - Primary ID KS0L-M
Device Regulatory Overview
The Prodia Select (Model/Catalog Number: KS0L-M) is a medical device manufactured by ABRASIVE TECHNOLOGY, INC.. This product is indexed under FDA Product Code / Category Classification DZP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KS0L-M
- Product Code / EMDN
- DZP
- Device Name
- Diamond Dental Bur
- Database Sync Date
- 2026-08-09 09:06:21
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Prodia Select?
The registered manufacturer of record for Prodia Select is ABRASIVE TECHNOLOGY, INC..
What is the Primary UDI-DI identifier for Prodia Select?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is KS0L-M.
What classification code is assigned to this device?
This device is registered under product classification code DZP.
Similar Classification Devices (DZP)
Other Devices by ABRASIVE TECHNOLOGY, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint