gudid
Primary ID: Blue Type 1
C-Warmer (UDI Blue Type 1)
Manufactured by DXM CO., LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C-Warmer - Primary ID Blue Type 1
Device Regulatory Overview
The C-Warmer (Model/Catalog Number: Blue Type 1) is a medical device manufactured by DXM CO., LTD. This product is indexed under FDA Product Code / Category Classification EFC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Blue Type 1
- Product Code / EMDN
- EFC
- Device Name
- C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled cartridge/composite warmer significantly reduces curing time with more flowability of composites and conveniently warms anesthetics and composites in one locations.
- Database Sync Date
- 2026-08-09 09:28:56
Full Regulatory Attributes
🔒 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 C-Warmer?
The registered manufacturer of record for C-Warmer is DXM CO., LTD.
What is the Primary UDI-DI identifier for C-Warmer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Blue Type 1.
What classification code is assigned to this device?
This device is registered under product classification code EFC.
Similar Classification Devices (EFC)
Other Devices by DXM CO., LTD
Programmatic Export
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JSON API Endpoint