GUDIDData
eudamed_udi Primary ID: 08057440230056

SIMPLEX 2 (UDI 08057440230056)

Manufactured by SLN SERVICE SRLS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SIMPLEX 2 - Primary ID 08057440230056

Device Regulatory Overview

The SIMPLEX 2 (Model/Catalog Number: 500/2) is a medical device manufactured by SLN SERVICE SRLS. This product is indexed under FDA Product Code / Category Classification V080602 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
500/2
Product Code / EMDN
V080602
Device Name
Letto con Regolazione Meccanica
Database Sync Date
2026-08-09 17:23:43

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SIMPLEX 2?

The registered manufacturer of record for SIMPLEX 2 is SLN SERVICE SRLS.

What is the Primary UDI-DI identifier for SIMPLEX 2?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057440230056.

What classification code is assigned to this device?

This device is registered under product classification code V080602.

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