eudamed_udi Primary ID: 05019829011734

Unspecified Brand (UDI 05019829011734)

Manufactured by Vernacare

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Unspecified Brand (Model/Catalog Number: AM200NCE) is a medical device manufactured by Vernacare. This product is indexed under FDA Product Code / Category Classification Z12011301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: AM200NCE
Product Code / EMDN: Z12011301
Device Name: 200 Wipes Azo Universal canister refill – CE marked
Database Sync Date: 2026-08-09 17:44:45

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 Unspecified Brand?

The registered manufacturer of record for Unspecified Brand is Vernacare.

What is the Primary UDI-DI identifier for Unspecified Brand?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05019829011734.

What classification code is assigned to this device?

This device is registered under product classification code Z12011301.

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