CardioGraphe (UDI 07290016484007)

Manufactured by Arineta

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CardioGraphe (Model/Catalog Number: 07290016484007) is a medical device manufactured by Arineta. This product is indexed under FDA Product Code / Category Classification Z11020301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 07290016484007
Product Code / EMDN: Z11020301
Device Name: SpotLight and CardioGraphe family of products
Database Sync Date: 2026-08-09 16:58:12

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 CardioGraphe?

The registered manufacturer of record for CardioGraphe is Arineta.

What is the Primary UDI-DI identifier for CardioGraphe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07290016484007.

What classification code is assigned to this device?

This device is registered under product classification code Z11020301.

Similar Classification Devices (Z11020301)

Programmatic Export

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

JSON API Endpoint