eudamed_udi
Primary ID: 08053876090875
Mbase Ti Abutment (UDI 08053876090875)
Manufactured by NEW ANCORVIS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Mbase Ti Abutment - Primary ID 08053876090875
Device Regulatory Overview
The Mbase Ti Abutment (Model/Catalog Number: MB3ICE34T-10) is a medical device manufactured by NEW ANCORVIS SRL. This product is indexed under FDA Product Code / Category Classification Q010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MB3ICE34T-10
- Product Code / EMDN
- Q010299
- Device Name
- Mbase Moncone
- Database Sync Date
- 2026-08-09 16:29:08
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 Mbase Ti Abutment?
The registered manufacturer of record for Mbase Ti Abutment is NEW ANCORVIS SRL.
What is the Primary UDI-DI identifier for Mbase Ti Abutment?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053876090875.
What classification code is assigned to this device?
This device is registered under product classification code Q010299.
Similar Classification Devices (Q010299)
Other Devices by NEW ANCORVIS SRL
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