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gudid Primary ID: SP-22850

Sample, Lighted Placement Tool (UDI SP-22850)

Manufactured by Bionix, LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sample, Lighted Placement Tool - Primary ID SP-22850

Device Regulatory Overview

The Sample, Lighted Placement Tool (Model/Catalog Number: SP-22850) is a medical device manufactured by Bionix, LLC. This product is indexed under FDA Product Code / Category Classification JYG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SP-22850
Product Code / EMDN
JYG
Device Name
Sample, Lighted Placement Tool
Database Sync Date
2026-08-09 09:04:11

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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Frequently Asked Questions

Who is the primary manufacturer of Sample, Lighted Placement Tool?

The registered manufacturer of record for Sample, Lighted Placement Tool is Bionix, LLC.

What is the Primary UDI-DI identifier for Sample, Lighted Placement Tool?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SP-22850.

What classification code is assigned to this device?

This device is registered under product classification code JYG.

Similar Classification Devices (JYG)

Other Devices by Bionix, LLC

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