GUDIDData
eudamed_udi Primary ID: 06973105239191

Splint (UDI 06973105239191)

Manufactured by Anping Guardian Medical Equipment Co., Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Splint - Primary ID 06973105239191

Device Regulatory Overview

The Splint (Model/Catalog Number: AZ-AB005B) is a medical device manufactured by Anping Guardian Medical Equipment Co., Ltd. This product is indexed under FDA Product Code / Category Classification M03050299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AZ-AB005B
Product Code / EMDN
M03050299
Device Name
Splint
Database Sync Date
2026-08-09 16:30:03

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 Splint?

The registered manufacturer of record for Splint is Anping Guardian Medical Equipment Co., Ltd.

What is the Primary UDI-DI identifier for Splint?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973105239191.

What classification code is assigned to this device?

This device is registered under product classification code M03050299.

Programmatic Export

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

JSON API Endpoint