GUDIDData
eudamed_udi Primary ID: 04542187240573

Sonda Sengstaken Blakemore (Tipo 42) (UDI 04542187240573)

Manufactured by CREATE MEDIC CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sonda Sengstaken Blakemore (Tipo 42) - Primary ID 04542187240573

Device Regulatory Overview

The Sonda Sengstaken Blakemore (Tipo 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 16:59:52

Full Regulatory Attributes

đź”’ 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 Sonda Sengstaken Blakemore (Tipo 42)?

The registered manufacturer of record for Sonda Sengstaken Blakemore (Tipo 42) is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Sonda Sengstaken Blakemore (Tipo 42)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187240573.

What classification code is assigned to this device?

This device is registered under product classification code G010201.

Programmatic Export

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

JSON API Endpoint