GUDIDData
eudamed_udi Primary ID: 08057440230094

MASSAGE 3 (UDI 08057440230094)

Manufactured by SLN SERVICE SRLS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MASSAGE 3 - Primary ID 08057440230094

Device Regulatory Overview

The MASSAGE 3 (Model/Catalog Number: 900/3) is a medical device manufactured by SLN SERVICE SRLS. This product is indexed under FDA Product Code / Category Classification V08060101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
900/3
Product Code / EMDN
V08060101
Device Name
Letto con Regolazione Elettrica
Database Sync Date
2026-08-09 16:58:50

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 MASSAGE 3?

The registered manufacturer of record for MASSAGE 3 is SLN SERVICE SRLS.

What is the Primary UDI-DI identifier for MASSAGE 3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057440230094.

What classification code is assigned to this device?

This device is registered under product classification code V08060101.

Programmatic Export

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

JSON API Endpoint