ACE (UDI 08034063842743)

Manufactured by FAR Srl

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ACE (Model/Catalog Number: CY02-36) is a medical device manufactured by FAR Srl. This product is indexed under FDA Product Code / Category Classification W01010109 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CY02-36
Product Code / EMDN: W01010109
Device Name: ACE
Database Sync Date: 2026-08-09 16:49:08

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 ACE?

The registered manufacturer of record for ACE is FAR Srl.

What is the Primary UDI-DI identifier for ACE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08034063842743.

What classification code is assigned to this device?

This device is registered under product classification code W01010109.

Similar Classification Devices (W01010109)

Other Devices by FAR Srl

Programmatic Export

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

JSON API Endpoint