GUDIDData
gudid Primary ID: SMR350

ECTphan (UDI SMR350)

Manufactured by Providus Holdings, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ECTphan - Primary ID SMR350

Device Regulatory Overview

The ECTphan (Model/Catalog Number: SMR350) is a medical device manufactured by Providus Holdings, Inc.. This product is indexed under FDA Product Code / Category Classification IXF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SMR350
Product Code / EMDN
IXF
Device Name
Solid "cold" low contrast rod with 20mm, 15mm, and 10mm ODs
Database Sync Date
2026-08-09 09:22:08

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 ECTphan?

The registered manufacturer of record for ECTphan is Providus Holdings, Inc..

What is the Primary UDI-DI identifier for ECTphan?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SMR350.

What classification code is assigned to this device?

This device is registered under product classification code IXF.

Programmatic Export

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

JSON API Endpoint