Moonizip (UDI 03770021793195)

Manufactured by Artis CF

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Moonizip (Model/Catalog Number: 1001) is a medical device manufactured by Artis CF. This product is indexed under FDA Product Code / Category Classification M030299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 1001
Product Code / EMDN: M030299
Device Name: Pansements en bambou
Database Sync Date: 2026-08-09 16:51:22

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 Moonizip?

The registered manufacturer of record for Moonizip is Artis CF.

What is the Primary UDI-DI identifier for Moonizip?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03770021793195.

What classification code is assigned to this device?

This device is registered under product classification code M030299.

Similar Classification Devices (M030299)

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