GUDIDData
eudamed_udi Primary ID: 05944760051191

TRIAMED, SENIOR 01, Lumbosacral orthosis (UDI 05944760051191)

Manufactured by SC TRIAMED SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRIAMED, SENIOR 01, Lumbosacral orthosis - Primary ID 05944760051191

Device Regulatory Overview

The TRIAMED, SENIOR 01, Lumbosacral orthosis (Model/Catalog Number: SRT120M2) is a medical device manufactured by SC TRIAMED SRL. This product is indexed under FDA Product Code / Category Classification Y060308 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SRT120M2
Product Code / EMDN
Y060308
Device Name
Spinal orthoses
Database Sync Date
2026-08-09 16:28:56

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 TRIAMED, SENIOR 01, Lumbosacral orthosis?

The registered manufacturer of record for TRIAMED, SENIOR 01, Lumbosacral orthosis is SC TRIAMED SRL.

What is the Primary UDI-DI identifier for TRIAMED, SENIOR 01, Lumbosacral orthosis?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05944760051191.

What classification code is assigned to this device?

This device is registered under product classification code Y060308.

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