761 (UDI 03615800000227)

Manufactured by VILGO

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

Scannable UDI-DI Representation

Device Regulatory Overview

The 761 (Model/Catalog Number: 1020015S1) is a medical device manufactured by VILGO. This product is indexed under FDA Product Code / Category Classification Y12030601 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1020015S1
Product Code / EMDN: Y12030601
Device Name: 761
Database Sync Date: 2026-08-09 16:29:25

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 761?

The registered manufacturer of record for 761 is VILGO.

What is the Primary UDI-DI identifier for 761?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03615800000227.

What classification code is assigned to this device?

This device is registered under product classification code Y12030601.

Similar Classification Devices (Y12030601)

Other Devices by VILGO

Programmatic Export

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

JSON API Endpoint