GUDIDData
gudid Primary ID: S-BMMUA4845

Implantswiss (UDI S-BMMUA4845)

Manufactured by Novodent SA

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Implantswiss - Primary ID S-BMMUA4845

Device Regulatory Overview

The Implantswiss (Model/Catalog Number: S-BMMUA4845) is a medical device manufactured by Novodent SA. This product is indexed under FDA Product Code / Category Classification NHA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
S-BMMUA4845
Product Code / EMDN
NHA
Device Name
Bone level Mini Multi Unit Abutment 4.8 x 4.5 mm Implant system for the support of dental prostheses, aimed at restoring missing teeth for aesthetical and functional purposes. Abutment: The part of the system that makes the link between the implant part and the prosthetic super structure.
Database Sync Date
2026-08-09 09:03:19

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Implantswiss?

The registered manufacturer of record for Implantswiss is Novodent SA.

What is the Primary UDI-DI identifier for Implantswiss?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S-BMMUA4845.

What classification code is assigned to this device?

This device is registered under product classification code NHA.

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