All Silicone Gastrostomy Balloon Catheter (Standard Type) (UDI 04542187212143)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The All Silicone Gastrostomy Balloon Catheter (Standard Type) (Model/Catalog Number: 800 000 1987) 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
- 800 000 1987
- Product Code / EMDN
- G02020201
- Device Name
- All Silicone Gastrostomy Balloon Catheter
- Database Sync Date
- 2026-08-09 16:47:06
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 All Silicone Gastrostomy Balloon Catheter (Standard Type)?
The registered manufacturer of record for All Silicone Gastrostomy Balloon Catheter (Standard Type) is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for All Silicone Gastrostomy Balloon Catheter (Standard Type)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187212143.
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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