gudid
Primary ID: 28200100
Max Bond LC Kit (UDI 28200100)
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 Max Bond LC Kit - Primary ID 28200100
Device Regulatory Overview
The Max Bond LC Kit (Model/Catalog Number: 28200100) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification KLE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 28200100
- Product Code / EMDN
- KLE
- Device Name
- Dental Bonding Agent
- 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 Max Bond LC Kit?
The registered manufacturer of record for Max Bond LC Kit is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for Max Bond LC Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 28200100.
What classification code is assigned to this device?
This device is registered under product classification code KLE.
Similar Classification Devices (KLE)
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