gudid Primary ID: AGR-AB

SHINING 3D (UDI AGR-AB)

Manufactured by Shining 3D Tech Co., Ltd.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SHINING 3D (Model/Catalog Number: AGR-AB) is a medical device manufactured by Shining 3D Tech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NOF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AGR-AB
Product Code / EMDN: NOF
Device Name
Database Sync Date: 2026-08-09 09:05:22

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of SHINING 3D?

The registered manufacturer of record for SHINING 3D is Shining 3D Tech Co., Ltd..

What is the Primary UDI-DI identifier for SHINING 3D?

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

What classification code is assigned to this device?

This device is registered under product classification code NOF.

Similar Classification Devices (NOF)

Other Devices by Shining 3D Tech Co., Ltd.

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