GUDIDData
eudamed_udi Primary ID: 06973245041937

Unspecified Brand (UDI 06973245041937)

Manufactured by Brun Medical Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06973245041937

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: BR-RAT3C) is a medical device manufactured by Brun Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification C90010301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
BR-RAT3C
Product Code / EMDN
C90010301
Device Name
Radial Artery Tourniquets
Database Sync Date
2026-08-09 16:28:56

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Brun Medical Co., Ltd..

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973245041937.

What classification code is assigned to this device?

This device is registered under product classification code C90010301.

Programmatic Export

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

JSON API Endpoint