Sonde de Gastrostomie de remplacement (UDI 04542187207835)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The Sonde de Gastrostomie de remplacement (Model/Catalog Number: EN800-000-2168) is a medical device manufactured by CREATE MEDIC CO., LTD.. This product is indexed under FDA Product Code / Category Classification G02020201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- EN800-000-2168
- Product Code / EMDN
- G02020201
- Device Name
- All Silicone Gastrostomy Balloon Catheter
- Database Sync Date
- 2026-08-09 16:45:40
Full Regulatory Attributes
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{
"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 Sonde de Gastrostomie de remplacement?
The registered manufacturer of record for Sonde de Gastrostomie de remplacement is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for Sonde de Gastrostomie de remplacement?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187207835.
What classification code is assigned to this device?
This device is registered under product classification code G02020201.
Similar Classification Devices (G02020201)
Other Devices by CREATE MEDIC CO., LTD.
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