gudid Primary ID: 1401-2723

Phaco Set Sophi - 23G/Curved (UDI 1401-2723)

Manufactured by This AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Phaco Set Sophi - 23G/Curved (Model/Catalog Number: 1401-2723) is a medical device manufactured by This AG. This product is indexed under FDA Product Code / Category Classification HQC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1401-2723
Product Code / EMDN: HQC
Device Name
Database Sync Date: 2026-08-09 09:03:20

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 Phaco Set Sophi - 23G/Curved?

The registered manufacturer of record for Phaco Set Sophi - 23G/Curved is This AG.

What is the Primary UDI-DI identifier for Phaco Set Sophi - 23G/Curved?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1401-2723.

What classification code is assigned to this device?

This device is registered under product classification code HQC.

Similar Classification Devices (HQC)

Other Devices by This AG

Programmatic Export

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

JSON API Endpoint