GUDIDData
gudid Primary ID: L5 557 ProStyle SF SLC Yoshida

Lares Research (UDI L5 557 ProStyle SF SLC Yoshida)

Manufactured by LARES RESEARCH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Lares Research - Primary ID L5 557 ProStyle SF SLC Yoshida

Device Regulatory Overview

The Lares Research (Model/Catalog Number: L5 557 ProStyle SF SLC Yoshida) is a medical device manufactured by LARES RESEARCH. This product is indexed under FDA Product Code / Category Classification EFB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
L5 557 ProStyle SF SLC Yoshida
Product Code / EMDN
EFB
Device Name
High-speed Handpiece, L5 557 ProStyle SF, Swivel, Fiber optic, Ceramic, Yoshida connection
Database Sync Date
2026-08-09 09:01:11

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 Lares Research?

The registered manufacturer of record for Lares Research is LARES RESEARCH.

What is the Primary UDI-DI identifier for Lares Research?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is L5 557 ProStyle SF SLC Yoshida.

What classification code is assigned to this device?

This device is registered under product classification code EFB.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint