gudid
Primary ID: 28100100
Silk Line Kit (UDI 28100100)
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 Silk Line Kit - Primary ID 28100100
Device Regulatory Overview
The Silk Line Kit (Model/Catalog Number: 28100100) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification EBI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28100100
- Product Code / EMDN
- EBI
- Device Name
- Soft Denture Relining Material
- 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 Silk Line Kit?
The registered manufacturer of record for Silk Line Kit is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for Silk Line Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28100100.
What classification code is assigned to this device?
This device is registered under product classification code EBI.
Similar Classification Devices (EBI)
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