GUDIDData
eudamed_udi Primary ID: 14711182606081

Silicone Hub-less Endo Drain Tube (UDI 14711182606081)

Manufactured by FORTUNE MEDICAL INSTRUMENT CORP.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Silicone Hub-less Endo Drain Tube - Primary ID 14711182606081

Device Regulatory Overview

The Silicone Hub-less Endo Drain Tube (Model/Catalog Number: 2015-0724) is a medical device manufactured by FORTUNE MEDICAL INSTRUMENT CORP.. This product is indexed under FDA Product Code / Category Classification A0601010402 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2015-0724
Product Code / EMDN
A0601010402
Device Name
Silicone Hub-less Endo Drain Tube
Database Sync Date
2026-08-09 16:48:41

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 Silicone Hub-less Endo Drain Tube?

The registered manufacturer of record for Silicone Hub-less Endo Drain Tube is FORTUNE MEDICAL INSTRUMENT CORP..

What is the Primary UDI-DI identifier for Silicone Hub-less Endo Drain Tube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14711182606081.

What classification code is assigned to this device?

This device is registered under product classification code A0601010402.

Programmatic Export

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

JSON API Endpoint