eudamed_udi Primary ID: 04542187225686

All Silicone Sengstaken Blakemore Tube (Type-42)　 (UDI 04542187225686)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The All Silicone Sengstaken Blakemore Tube (Type-42)　 (Model/Catalog Number: 002-182-0420) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 002-182-0420
Product Code / EMDN: G010201
Device Name: All Silicone Sengstaken Blakemore Tube
Database Sync Date: 2026-08-09 16:59:30

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 All Silicone Sengstaken Blakemore Tube (Type-42)　?

The registered manufacturer of record for All Silicone Sengstaken Blakemore Tube (Type-42)　 is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for All Silicone Sengstaken Blakemore Tube (Type-42)　?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187225686.

What classification code is assigned to this device?

This device is registered under product classification code G010201.

Similar Classification Devices (G010201)

Other Devices by CREATE MEDIC CO., LTD.

Programmatic Export

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

JSON API Endpoint

All Silicone Sengstaken Blakemore Tube (Type-42) (UDI 04542187225686)