gudid
Primary ID: 23100550
CF Carbon Fiber Post Kit (UDI 23100550)
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 CF Carbon Fiber Post Kit - Primary ID 23100550
Device Regulatory Overview
The CF Carbon Fiber Post Kit (Model/Catalog Number: 23100550) is a medical device manufactured by J. MORITA U.S.A., INC. This product is indexed under FDA Product Code / Category Classification ELR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 23100550
- Product Code / EMDN
- ELR
- Device Name
- Carbon Fiber Post used for core build up
- Database Sync Date
- 2026-08-09 09:49:34
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 CF Carbon Fiber Post Kit?
The registered manufacturer of record for CF Carbon Fiber Post Kit is J. MORITA U.S.A., INC.
What is the Primary UDI-DI identifier for CF Carbon Fiber Post Kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 23100550.
What classification code is assigned to this device?
This device is registered under product classification code ELR.
Similar Classification Devices (ELR)
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