eudamed_udi Primary ID: 05060614531272

Alerta Bubble 2 Overlay Low Risk (Euro Plug) (UDI 05060614531272)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Alerta Bubble 2 Overlay Low Risk (Euro Plug) (Model/Catalog Number: ALT-9001/EU) is a medical device manufactured by Alerta Medical Ltd. This product is indexed under FDA Product Code / Category Classification V08068099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ALT-9001/EU
Product Code / EMDN: V08068099
Device Name: Alerta Partner Cushion System
Database Sync Date: 2026-08-09 16:46:43

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of Alerta Bubble 2 Overlay Low Risk (Euro Plug)?

The registered manufacturer of record for Alerta Bubble 2 Overlay Low Risk (Euro Plug) is Alerta Medical Ltd.

What is the Primary UDI-DI identifier for Alerta Bubble 2 Overlay Low Risk (Euro Plug)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05060614531272.

What classification code is assigned to this device?

This device is registered under product classification code V08068099.

Similar Classification Devices (V08068099)

Other Devices by Alerta Medical Ltd

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint