ACEMST1 (UDI ACEMST1.1 /RR)

Manufactured by ACEM SPA

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

Scannable UDI-DI Representation

Device Regulatory Overview

The ACEMST1 (Model/Catalog Number: ACEMST1.1 /RR) is a medical device manufactured by ACEM SPA. This product is indexed under FDA Product Code / Category Classification KZF within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: ACEMST1.1 /RR
Product Code / EMDN: KZF
Device Name: ACEMST1.1 ARTICULATED ARM RAIL
Database Sync Date: 2026-08-09 09:04:32

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 ACEMST1?

The registered manufacturer of record for ACEMST1 is ACEM SPA.

What is the Primary UDI-DI identifier for ACEMST1?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ACEMST1.1 /RR.

What classification code is assigned to this device?

This device is registered under product classification code KZF.

Similar Classification Devices (KZF)

Other Devices by ACEM SPA

Programmatic Export

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

JSON API Endpoint