eudamed_udi Primary ID: 08595605204196

ActiveGel (UDI 08595605204196)

Manufactured by ALPA, a.s.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The ActiveGel (Model/Catalog Number: N/A) is a medical device manufactured by ALPA, a.s.. This product is indexed under FDA Product Code / Category Classification Z12069099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: N/A
Product Code / EMDN: Z12069099
Device Name: ALPA Active gel hřebíček
Database Sync Date: 2026-08-09 16:29:13

Full Regulatory Attributes

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{
    "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 ActiveGel?

The registered manufacturer of record for ActiveGel is ALPA, a.s..

What is the Primary UDI-DI identifier for ActiveGel?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08595605204196.

What classification code is assigned to this device?

This device is registered under product classification code Z12069099.

Similar Classification Devices (Z12069099)

Other Devices by ALPA, a.s.

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