PEG REPLACEMENT WITH ENFIT CONNECTOR (UDI 04542187172676)
Manufactured by CREATE MEDIC CO., LTD.
Device Regulatory Overview
The PEG REPLACEMENT WITH ENFIT CONNECTOR (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 16:51:13
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 PEG REPLACEMENT WITH ENFIT CONNECTOR?
The registered manufacturer of record for PEG REPLACEMENT WITH ENFIT CONNECTOR is CREATE MEDIC CO., LTD..
What is the Primary UDI-DI identifier for PEG REPLACEMENT WITH ENFIT CONNECTOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04542187172676.
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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