GUDIDData
gudid Primary ID: 508-560

FORD DIXON LIGATOR (UDI 508-560)

Manufactured by SONTEC INSTRUMENTS, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FORD DIXON LIGATOR - Primary ID 508-560

Device Regulatory Overview

The FORD DIXON LIGATOR (Model/Catalog Number: 508-560) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification FHN within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
508-560
Product Code / EMDN
FHN
Device Name
FORD DIXON LIGATOR WITH LOADING CONE & 100 O-RINGS
Database Sync Date
2026-08-09 09:07:04

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 FORD DIXON LIGATOR?

The registered manufacturer of record for FORD DIXON LIGATOR is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for FORD DIXON LIGATOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 508-560.

What classification code is assigned to this device?

This device is registered under product classification code FHN.

Programmatic Export

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

JSON API Endpoint