eudamed_udi Primary ID: G796PI04700

Double-Ended Ligature Director 17.5cm (UDI G796PI04700)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Double-Ended Ligature Director 17.5cm (Model/Catalog Number: PI0470) is a medical device manufactured by Promed Instruments. This product is indexed under FDA Product Code / Category Classification L159009 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: PI0470
Product Code / EMDN: L159009
Device Name: Double-Ended Ligature Director 17.5cm
Database Sync Date: 2026-08-09 16:46:06

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 Double-Ended Ligature Director 17.5cm?

The registered manufacturer of record for Double-Ended Ligature Director 17.5cm is Promed Instruments.

What is the Primary UDI-DI identifier for Double-Ended Ligature Director 17.5cm?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is G796PI04700.

What classification code is assigned to this device?

This device is registered under product classification code L159009.

Similar Classification Devices (L159009)

Other Devices by Promed Instruments

Programmatic Export

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

JSON API Endpoint