GUDIDData
gudid Primary ID: Komet BioRepair 1.5 g

Komet BioRepair (UDI Komet BioRepair 1.5 g)

Manufactured by Angelus Industria de Produtos Odontologicos S A

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Komet BioRepair - Primary ID Komet BioRepair 1.5 g

Device Regulatory Overview

The Komet BioRepair (Model/Catalog Number: Komet BioRepair 1.5 g) is a medical device manufactured by Angelus Industria de Produtos Odontologicos S A. This product is indexed under FDA Product Code / Category Classification KIF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
Komet BioRepair 1.5 g
Product Code / EMDN
KIF
Device Name
Bioceramic reparative material ready-to-use.
Database Sync Date
2026-08-09 09:07:20

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 Komet BioRepair?

The registered manufacturer of record for Komet BioRepair is Angelus Industria de Produtos Odontologicos S A.

What is the Primary UDI-DI identifier for Komet BioRepair?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Komet BioRepair 1.5 g.

What classification code is assigned to this device?

This device is registered under product classification code KIF.

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