gudid Primary ID: 355-265

BONE GRINDER (UDI 355-265)

Manufactured by SONTEC INSTRUMENTS, INC.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The BONE GRINDER (Model/Catalog Number: 355-265) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification LYS within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 355-265
Product Code / EMDN: LYS
Device Name: BONE GRINDER
Database Sync Date: 2026-08-09 09:07:05

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 BONE GRINDER?

The registered manufacturer of record for BONE GRINDER is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for BONE GRINDER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 355-265.

What classification code is assigned to this device?

This device is registered under product classification code LYS.

Similar Classification Devices (LYS)

Other Devices by SONTEC INSTRUMENTS, INC.

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