gudid
Primary ID: 10814832014626B
Efferdent (UDI 10814832014626B)
Manufactured by Medtech Products Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Efferdent - Primary ID 10814832014626B
Device Regulatory Overview
The Efferdent (Model/Catalog Number: 10814832014626B) is a medical device manufactured by Medtech Products Inc.. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10814832014626B
- Product Code / EMDN
- EFT
- Device Name
- Efferdent Fresh Guard Soak 24CT
- Database Sync Date
- 2026-08-09 09:40:23
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Efferdent?
The registered manufacturer of record for Efferdent is Medtech Products Inc..
What is the Primary UDI-DI identifier for Efferdent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10814832014626B.
What classification code is assigned to this device?
This device is registered under product classification code EFT.
Similar Classification Devices (EFT)
Other Devices by Medtech Products Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint