GUDIDData
eudamed_udi Primary ID: 04542187216592

Sonda Sengstaken Blakemore din silicon tip (UDI 04542187216592)

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 din silicon tip - Primary ID 04542187216592

Device Regulatory Overview

The Sonda Sengstaken Blakemore din silicon tip (Model/Catalog Number: NS800 320 0210) 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
NS800 320 0210
Product Code / EMDN
G010201
Device Name
All Silicone Sengstaken Blakemore Tube
Database Sync Date
2026-08-09 16:50:11

Full Regulatory Attributes

đź”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Sonda Sengstaken Blakemore din silicon tip?

The registered manufacturer of record for Sonda Sengstaken Blakemore din silicon tip is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Sonda Sengstaken Blakemore din silicon tip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187216592.

What classification code is assigned to this device?

This device is registered under product classification code G010201.

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