GUDIDData
gudid Primary ID: 220700

Constic A1 (UDI 220700)

Manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Constic A1 - Primary ID 220700

Device Regulatory Overview

The Constic A1 (Model/Catalog Number: 220700) is a medical device manufactured by DMG Chemisch-Pharmazeutische Fabrik GmbH. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
220700
Product Code / EMDN
EBF
Device Name
Self-adhesive, light-curing, flowable composite. Do more with less. Content: 2 syringes @ 2g composite, accessories. Color: A1.
Database Sync Date
2026-08-09 09:23:50

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 Constic A1?

The registered manufacturer of record for Constic A1 is DMG Chemisch-Pharmazeutische Fabrik GmbH.

What is the Primary UDI-DI identifier for Constic A1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 220700.

What classification code is assigned to this device?

This device is registered under product classification code EBF.

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