gudid
Primary ID: 28700100
FormCore DC (UDI 28700100)
Manufactured by J. MORITA U.S.A., INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FormCore DC - Primary ID 28700100
Device Regulatory Overview
The FormCore DC (Model/Catalog Number: 28700100) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28700100
- Product Code / EMDN
- EBF
- Device Name
- Dental Composite Resin for Core Build-up
- Database Sync Date
- 2026-08-09 09:58:58
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 FormCore DC?
The registered manufacturer of record for FormCore DC is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for FormCore DC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28700100.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
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