GUDIDData
eudamed_udi Primary ID: 05944760054116

TRIAMED, TRIAFIX MANU, Fixed wrist hand brace (UDI 05944760054116)

Manufactured by SC TRIAMED SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRIAMED, TRIAFIX MANU, Fixed wrist hand brace - Primary ID 05944760054116

Device Regulatory Overview

The TRIAMED, TRIAFIX MANU, Fixed wrist hand brace (Model/Catalog Number: SRT229M5R) is a medical device manufactured by SC TRIAMED SRL. This product is indexed under FDA Product Code / Category Classification Y060612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SRT229M5R
Product Code / EMDN
Y060612
Device Name
UPPER LIMB 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, TRIAFIX MANU, Fixed wrist hand brace?

The registered manufacturer of record for TRIAMED, TRIAFIX MANU, Fixed wrist hand brace is SC TRIAMED SRL.

What is the Primary UDI-DI identifier for TRIAMED, TRIAFIX MANU, Fixed wrist hand brace?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05944760054116.

What classification code is assigned to this device?

This device is registered under product classification code Y060612.

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