gudid Primary ID: NA

Cannulated Universal Quick Connect Handle (UDI NA)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Cannulated Universal Quick Connect Handle (Model/Catalog Number: NA) is a medical device manufactured by TOBY ORTHOPAEDICS. This product is indexed under FDA Product Code / Category Classification HXX within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: NA
Product Code / EMDN: HXX
Device Name: Drivers are of various tips and handle geometry and are made of stainless steel that is heat treated and passivated. Driver assembly handles are made from machined Radel.
Database Sync Date: 2026-08-09 09:40:13

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 Cannulated Universal Quick Connect Handle?

The registered manufacturer of record for Cannulated Universal Quick Connect Handle is TOBY ORTHOPAEDICS.

What is the Primary UDI-DI identifier for Cannulated Universal Quick Connect Handle?

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 HXX.

Similar Classification Devices (HXX)

Other Devices by TOBY ORTHOPAEDICS

Programmatic Export

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

JSON API Endpoint