GUDIDData
eudamed_udi Primary ID: 05944760052983

TRIAMED, CARPOFIX M FINGER, Fixed wrist hand finger orthosis (UDI 05944760052983)

Manufactured by SC TRIAMED SRL

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TRIAMED, CARPOFIX M FINGER, Fixed wrist hand finger orthosis - Primary ID 05944760052983

Device Regulatory Overview

The TRIAMED, CARPOFIX M FINGER, Fixed wrist hand finger orthosis (Model/Catalog Number: SRT212M3L) is a medical device manufactured by SC TRIAMED SRL. This product is indexed under FDA Product Code / Category Classification Y060613 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
SRT212M3L
Product Code / EMDN
Y060613
Device Name
UPPER LIMB ORTHOSES
Database Sync Date
2026-08-09 16:28:57

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, CARPOFIX M FINGER, Fixed wrist hand finger orthosis?

The registered manufacturer of record for TRIAMED, CARPOFIX M FINGER, Fixed wrist hand finger orthosis is SC TRIAMED SRL.

What is the Primary UDI-DI identifier for TRIAMED, CARPOFIX M FINGER, Fixed wrist hand finger orthosis?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05944760052983.

What classification code is assigned to this device?

This device is registered under product classification code Y060613.

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