GUDIDData
eudamed_udi Primary ID: J017A62L15L40

VITAPAN® (UDI J017A62L15L40)

Manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VITAPAN® - Primary ID J017A62L15L40

Device Regulatory Overview

The VITAPAN® (Model/Catalog Number: A62L15L4) is a medical device manufactured by VITA Zahnfabrik H. Rauter GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Q010699 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
A62L15L4
Product Code / EMDN
Q010699
Device Name
Artificial teeth
Database Sync Date
2026-08-09 16:28:47

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 VITAPAN®?

The registered manufacturer of record for VITAPAN® is VITA Zahnfabrik H. Rauter GmbH & Co. KG.

What is the Primary UDI-DI identifier for VITAPAN®?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J017A62L15L40.

What classification code is assigned to this device?

This device is registered under product classification code Q010699.

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