Medisoft (UDI 870 S)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Medisoft (Model/Catalog Number: 870 S) is a medical device manufactured by MEDISOFT RAM ITALIA SRL. This product is indexed under FDA Product Code / Category Classification IOL within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 870 S
Product Code / EMDN: IOL
Device Name: Treadmill 870 S
Database Sync Date: 2026-08-09 09:03:53

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 Medisoft?

The registered manufacturer of record for Medisoft is MEDISOFT RAM ITALIA SRL.

What is the Primary UDI-DI identifier for Medisoft?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 870 S.

What classification code is assigned to this device?

This device is registered under product classification code IOL.

Similar Classification Devices (IOL)

Other Devices by MEDISOFT RAM ITALIA SRL

Programmatic Export

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

JSON API Endpoint