GUDIDData
gudid Primary ID: 66079658

Pala (UDI 66079658)

Manufactured by Kulzer GmbH

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pala - Primary ID 66079658

Device Regulatory Overview

The Pala (Model/Catalog Number: 66079658) is a medical device manufactured by Kulzer GmbH. This product is indexed under FDA Product Code / Category Classification EFT within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
66079658
Product Code / EMDN
EFT
Device Name
Pala Brillance Denture Cleanser 2 ct. sample
Database Sync Date
2026-08-09 09:09:38

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 Pala?

The registered manufacturer of record for Pala is Kulzer GmbH.

What is the Primary UDI-DI identifier for Pala?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 66079658.

What classification code is assigned to this device?

This device is registered under product classification code EFT.

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