GUDIDData
eudamed_udi Primary ID: 08053847360204

FLOW CANNULA XS Double Inspiratory Loop Cannula DILC (UDI 08053847360204)

Manufactured by GINEVRI srl

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FLOW CANNULA XS Double Inspiratory Loop Cannula DILC - Primary ID 08053847360204

Device Regulatory Overview

The FLOW CANNULA XS Double Inspiratory Loop Cannula DILC (Model/Catalog Number: 13230B73) is a medical device manufactured by GINEVRI srl. This product is indexed under FDA Product Code / Category Classification R0301020302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
13230B73
Product Code / EMDN
R0301020302
Device Name
FLOW CANNULA
Database Sync Date
2026-08-09 17:54:18

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 FLOW CANNULA XS Double Inspiratory Loop Cannula DILC?

The registered manufacturer of record for FLOW CANNULA XS Double Inspiratory Loop Cannula DILC is GINEVRI srl.

What is the Primary UDI-DI identifier for FLOW CANNULA XS Double Inspiratory Loop Cannula DILC?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053847360204.

What classification code is assigned to this device?

This device is registered under product classification code R0301020302.

Programmatic Export

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

JSON API Endpoint