gudid
Primary ID: 10.13.002
Morelli (UDI 10.13.002)
Manufactured by Dental Morelli Ltda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Morelli - Primary ID 10.13.002
Device Regulatory Overview
The Morelli (Model/Catalog Number: 10.13.002) is a medical device manufactured by Dental Morelli Ltda. This product is indexed under FDA Product Code / Category Classification EJF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10.13.002
- Product Code / EMDN
- EJF
- Device Name
- Bracket Prescription Roth - SLP .022" - 21
- Database Sync Date
- 2026-08-09 09:00:28
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 Morelli?
The registered manufacturer of record for Morelli is Dental Morelli Ltda.
What is the Primary UDI-DI identifier for Morelli?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10.13.002.
What classification code is assigned to this device?
This device is registered under product classification code EJF.
Similar Classification Devices (EJF)
Other Devices by Dental Morelli Ltda
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