gudid Primary ID: NA

5.2mm Cannulated Post, 35mm (UDI NA)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 5.2mm Cannulated Post, 35mm (Model/Catalog Number: NA) is a medical device manufactured by TOBY ORTHOPAEDICS. This product is indexed under FDA Product Code / Category Classification HWC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NA
Product Code / EMDN: HWC
Device Name: Titanium alloy posts are used to affix the proximal end of the plate to the proximal end of the humerus. With the aid of fixtures, the posts have the ability to have cross elements inserted perpendicular to the axis of the cortical thread of the post. The head of the post is a threaded locking configuration that accepts an expansion cap screw. The posts are 5.25mm in diameter and are available in 5 lengths ranging from 30mm to 50mm. They are cannulated i.e a K-wire can pass through the post longitudinally.
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 5.2mm Cannulated Post, 35mm?

The registered manufacturer of record for 5.2mm Cannulated Post, 35mm is TOBY ORTHOPAEDICS.

What is the Primary UDI-DI identifier for 5.2mm Cannulated Post, 35mm?

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 HWC.

Similar Classification Devices (HWC)

Other Devices by TOBY ORTHOPAEDICS

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