GUDIDData
eudamed_udi Primary ID: 04542187228854

Sengstaken Blakemore Sonde aus Silikon (Typ 32) (UDI 04542187228854)

Manufactured by CREATE MEDIC CO., LTD.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sengstaken Blakemore Sonde aus Silikon (Typ 32) - Primary ID 04542187228854

Device Regulatory Overview

The Sengstaken Blakemore Sonde aus Silikon (Typ 32) (Model/Catalog Number: 800 320 0140) 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
800 320 0140
Product Code / EMDN
G010201
Device Name
All Silicone Sengstaken Blakemore Tube
Database Sync Date
2026-08-09 16:50:49

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 Sengstaken Blakemore Sonde aus Silikon (Typ 32)?

The registered manufacturer of record for Sengstaken Blakemore Sonde aus Silikon (Typ 32) is CREATE MEDIC CO., LTD..

What is the Primary UDI-DI identifier for Sengstaken Blakemore Sonde aus Silikon (Typ 32)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187228854.

What classification code is assigned to this device?

This device is registered under product classification code G010201.

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