gudid Primary ID: 10-255-25

Hu-Friedy (UDI 10-255-25)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Hu-Friedy (Model/Catalog Number: 10-255-25) is a medical device manufactured by HU-FRIEDY MFG. CO., LLC. This product is indexed under FDA Product Code / Category Classification GES within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 10-255-25
Product Code / EMDN: GES
Device Name: (Bx of 100) #25 Sterile Blade
Database Sync Date: 2026-08-09 09:17:35

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 Hu-Friedy?

The registered manufacturer of record for Hu-Friedy is HU-FRIEDY MFG. CO., LLC.

What is the Primary UDI-DI identifier for Hu-Friedy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-255-25.

What classification code is assigned to this device?

This device is registered under product classification code GES.

Similar Classification Devices (GES)

Other Devices by HU-FRIEDY MFG. CO., LLC

Programmatic Export

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

JSON API Endpoint