gudid Primary ID: NA

WOLF Instrument Sterilization Tray (UDI NA)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The WOLF Instrument Sterilization Tray (Model/Catalog Number: NA) is a medical device manufactured by TOBY ORTHOPAEDICS. This product is indexed under FDA Product Code / Category Classification LRP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NA
Product Code / EMDN: LRP
Device Name: Sterilization Tray for WOLF Instruments and Screw Caddy/Caddies.
Database Sync Date: 2026-08-09 09:40:13

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 WOLF Instrument Sterilization Tray?

The registered manufacturer of record for WOLF Instrument Sterilization Tray is TOBY ORTHOPAEDICS.

What is the Primary UDI-DI identifier for WOLF Instrument Sterilization Tray?

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

What classification code is assigned to this device?

This device is registered under product classification code LRP.

Similar Classification Devices (LRP)

Other Devices by TOBY ORTHOPAEDICS

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