GUDIDData
eudamed_udi Primary ID: 03322541080714

MADRID BLEU T40 (UDI 03322541080714)

Manufactured by GIBAUD

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MADRID BLEU T40 - Primary ID 03322541080714

Device Regulatory Overview

The MADRID BLEU T40 (Model/Catalog Number: 8451-40) is a medical device manufactured by GIBAUD. This product is indexed under FDA Product Code / Category Classification Y063303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8451-40
Product Code / EMDN
Y063303
Device Name
ATHENES beige T35
Database Sync Date
2026-08-09 16:28:46

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 MADRID BLEU T40?

The registered manufacturer of record for MADRID BLEU T40 is GIBAUD.

What is the Primary UDI-DI identifier for MADRID BLEU T40?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03322541080714.

What classification code is assigned to this device?

This device is registered under product classification code Y063303.

Programmatic Export

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

JSON API Endpoint