gudid
Primary ID: 1
Repair-it (UDI 1)
Manufactured by Doc Brands, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Repair-it - Primary ID 1
Device Regulatory Overview
The Repair-it (Model/Catalog Number: 1) is a medical device manufactured by Doc Brands, Inc.. This product is indexed under FDA Product Code / Category Classification EBO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- EBO
- Device Name
- Repair-it is an OTC denture repair kit for home use. The device consists of a material, such as a resin monomer system of powder and liquid glues, that is intended to be applied permanently to a denture to mend cracks or breaks.
- Database Sync Date
- 2026-08-09 09:00:34
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 Repair-it?
The registered manufacturer of record for Repair-it is Doc Brands, Inc..
What is the Primary UDI-DI identifier for Repair-it?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code EBO.
Similar Classification Devices (EBO)
Other Devices by Doc Brands, Inc.
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