eudamed_udi
Primary ID: 08053876013560
MUA (Multi Unit Abutment) 4.8 (UDI 08053876013560)
Manufactured by NEW ANCORVIS SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MUA (Multi Unit Abutment) 4.8 - Primary ID 08053876013560
Device Regulatory Overview
The MUA (Multi Unit Abutment) 4.8 (Model/Catalog Number: ILSCOS402I) 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
- ILSCOS402I
- Product Code / EMDN
- Q010299
- Device Name
- MUA (Multi Unit Abutment)
- 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 MUA (Multi Unit Abutment) 4.8?
The registered manufacturer of record for MUA (Multi Unit Abutment) 4.8 is NEW ANCORVIS SRL.
What is the Primary UDI-DI identifier for MUA (Multi Unit Abutment) 4.8?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053876013560.
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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