GUDIDData
gudid Primary ID: 5031-24-0-000-00

Quick Lock-3G-912-M8-S2 (UDI 5031-24-0-000-00)

Manufactured by Amtrion GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Quick Lock-3G-912-M8-S2 - Primary ID 5031-24-0-000-00

Device Regulatory Overview

The Quick Lock-3G-912-M8-S2 (Model/Catalog Number: 5031-24-0-000-00) is a medical device manufactured by Amtrion GmbH. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
5031-24-0-000-00
Product Code / EMDN
JAY
Device Name
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 Quick Lock-3G-912-M8-S2?

The registered manufacturer of record for Quick Lock-3G-912-M8-S2 is Amtrion GmbH.

What is the Primary UDI-DI identifier for Quick Lock-3G-912-M8-S2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5031-24-0-000-00.

What classification code is assigned to this device?

This device is registered under product classification code JAY.

Programmatic Export

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

JSON API Endpoint