gudid Primary ID: 520-565

HEGAR UTERINE DILATOR SET (UDI 520-565)

Manufactured by SONTEC INSTRUMENTS, INC.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The HEGAR UTERINE DILATOR SET (Model/Catalog Number: 520-565) is a medical device manufactured by SONTEC INSTRUMENTS, INC.. This product is indexed under FDA Product Code / Category Classification HDQ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 520-565
Product Code / EMDN: HDQ
Device Name: HEGAR UTERINE DILATOR SET
Database Sync Date: 2026-08-09 09:07:02

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 HEGAR UTERINE DILATOR SET?

The registered manufacturer of record for HEGAR UTERINE DILATOR SET is SONTEC INSTRUMENTS, INC..

What is the Primary UDI-DI identifier for HEGAR UTERINE DILATOR SET?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 520-565.

What classification code is assigned to this device?

This device is registered under product classification code HDQ.

Similar Classification Devices (HDQ)

Other Devices by SONTEC INSTRUMENTS, INC.

Programmatic Export

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

JSON API Endpoint