All Silicone Sengstaken Blakemore Tube (Type 32) (UDI 04542187228793)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The All Silicone Sengstaken Blakemore Tube (Type 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 16:45:47
Full Regulatory Attributes
đź”’ Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of All Silicone Sengstaken Blakemore Tube (Type 32)?
The registered manufacturer of record for All Silicone Sengstaken Blakemore Tube (Type 32) is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for All Silicone Sengstaken Blakemore Tube (Type 32)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187228793.
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.
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