gudid Primary ID: D48-B

SHINING 3D (UDI D48-B)

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: D48-B) is a medical device manufactured by Shining 3D Tech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification NDP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: D48-B
Product Code / EMDN: NDP
Device Name
Database Sync Date: 2026-08-09 09:05:22

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 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 D48-B.

What classification code is assigned to this device?

This device is registered under product classification code NDP.

Similar Classification Devices (NDP)

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

Programmatic Export

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

JSON API Endpoint