GUDIDData
eudamed_udi Primary ID: 03666256012661

Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m (UDI 03666256012661)

Manufactured by Int'Air Médical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m - Primary ID 03666256012661

Device Regulatory Overview

The Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m (Model/Catalog Number: D305PC8X12) is a medical device manufactured by Int'Air Médical. This product is indexed under FDA Product Code / Category Classification R0580 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
D305PC8X12
Product Code / EMDN
R0580
Device Name
Dispositifs et accessoires d'aspiration non stériles
Database Sync Date
2026-08-09 16:30:01

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 Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m?

The registered manufacturer of record for Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m is Int'Air Médical.

What is the Primary UDI-DI identifier for Tube d'aspiration cristal 8 x12 mm, rouleau de 50 m?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03666256012661.

What classification code is assigned to this device?

This device is registered under product classification code R0580.

Programmatic Export

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

JSON API Endpoint