Neodent (UDI 116.305)
Manufactured by JJGC Indstria e Comrcio de Materiais Dentrios S/A.
Device Regulatory Overview
The Neodent (Model/Catalog Number: 116.305) is a medical device manufactured by JJGC Indstria e Comrcio de Materiais Dentrios S/A.. This product is indexed under FDA Product Code / Category Classification NHA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 116.305
- Product Code / EMDN
- NHA
- Device Name
- NGM ASC SCREW, TI
- Database Sync Date
- 2026-08-09 09:07:12
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 Neodent?
The registered manufacturer of record for Neodent is JJGC Indstria e Comrcio de Materiais Dentrios S/A..
What is the Primary UDI-DI identifier for Neodent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 116.305.
What classification code is assigned to this device?
This device is registered under product classification code NHA.
Similar Classification Devices (NHA)
Other Devices by JJGC Indstria e Comrcio de Materiais Dentrios S/A.
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